PRESSURE BIOSCIENCES INC - Quarter Report: 2008 March (Form 10-Q)
UNITED
STATES
SECURITIES
AND EXCHANGE COMMISSION
Washington,
D.C. 20549
FORM
10-Q
(Mark
One)
x
Quarterly Report Pursuant to Section 13 or 15(d) of the Securities Exchange
Act
of 1934
For
the quarterly period ended
March
31, 2008
or
o
Transition Report Pursuant to Section 13 or 15(d) of the Securities Exchange
Act
of 1934
For
the transition period from _____________ to _____________
Commission
file number
0-21615
PRESSURE
BIOSCIENCES, INC.
(Exact
Name of Registrant as Specified in its Charter)
Massachusetts
|
|
04-2652826
|
(State
or Other Jurisdiction of
|
|
(I.R.S.
Employer
|
Incorporation
or Organization)
|
|
Identification
No.)
|
14
Norfolk Avenue
South
Easton, Massachusetts
(Address
of Principal Executive Offices)
02375
(Zip
Code)
(508)
230-1828
(Registrant’s
Telephone Number, Including Area Code)
Indicate
by check mark whether the registrant (1) has filed all reports required to
be
filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during
the
preceding 12 months (or for such shorter period that the registrant was required
to file such reports), and (2) has been subject to such filing requirements
for
the past 90 days.
x Yes
o
No
Indicate
by check mark whether the registrant is a shell company (as defined in Exchange
Act Rule 12b-2 of the Exchange Act).
o
Yes x
No
The
number of shares outstanding of the Issuer’s common stock as of May 1, 2008 was
2,192,175
*Indicate
by check mark whether the registrant is a large accelerated filer, an
accelerated filer, a non-accelerated filer, or a smaller reporting company.
See
the definitions of “large accelerated filer,” “accelerated filer” and “smaller
reporting company” in Rule 12b-2 of the Exchange Act. (Check one):
Large
accelerated filer o
|
Accelerated
filer o
|
Non-accelerated
filer o
|
Smaller
reporting company x
|
TABLE
OF
CONTENTS
|
Page
|
PART
I - FINANCIAL INFORMATION
|
|
|
|
Item
1. Financial Statements (Unaudited)
|
|
Consolidated
Balance Sheets as of March 31, 2008 and December 31, 2007
|
1
|
|
|
Consolidated
Statements of Operations for the Three Months Ended March 31, 2008
and
2007
|
2
|
|
|
Consolidated
Statements of Comprehensive Loss for the Three Months Ended March
31, 2008
and 2007
|
3
|
|
|
Consolidated
Statements of Cash Flows for the Three Months Ended March 31, 2008
and
2007
|
4
|
|
|
Notes
to Consolidated Financial Statements
|
5
|
|
|
Item
2. Management's Discussion and Analysis of Financial Condition
and Results
of Operations
|
14
|
|
|
Item
4T. Controls and Procedures
|
22
|
|
|
PART
II - OTHER INFORMATION
|
|
|
|
Item
6. Exhibits
|
23
|
Item
1. Financial Statements
PRESSURE
BIOSCIENCES, INC. AND SUBSIDIARIES
CONSOLIDATED
BALANCE SHEETS
(UNAUDITED)
March
31,
|
December
31,
|
||||||
2008
|
2007
|
||||||
ASSETS
|
|||||||
CURRENT
ASSETS
|
|
|
|||||
Cash
and cash equivalents
|
$
|
4,146,820
|
$
|
5,424,486
|
|||
Accounts
receivable
|
106,867
|
118,471
|
|||||
Inventories
|
595,060
|
172,548
|
|||||
Deposits
|
211,561
|
553,483
|
|||||
Prepaid
income taxes
|
58,463
|
56,863
|
|||||
Income
tax receivable
|
249,541
|
249,541
|
|||||
Prepaid
expenses and other current assets
|
220,407
|
94,783
|
|||||
Total
current assets
|
5,588,719
|
6,670,175
|
|||||
|
|
|
|||||
PROPERTY
AND EQUIPMENT, NET
|
339,713
|
257,797
|
|||||
|
|
|
|||||
OTHER
ASSETS
|
|
|
|||||
Intangible
assets, net
|
316,132
|
328,290
|
|||||
TOTAL
ASSETS
|
$
|
6,244,564
|
$
|
7,256,262
|
|||
|
|
|
|||||
LIABILITIES
AND STOCKHOLDERS' EQUITY
|
|
|
|||||
|
|
|
|||||
CURRENT
LIABILITIES
|
|
|
|||||
Accounts
payable
|
$
|
378,609
|
$
|
152,729
|
|||
Accrued
employee compensation
|
364,144
|
377,190
|
|||||
Accrued
professional fees and other expenses
|
189,642
|
186,840
|
|||||
Income
taxes payable
|
5,889
|
4,519
|
|||||
Deferred
revenue
|
9,911
|
15,075
|
|||||
Total
current liabilities
|
948,195
|
736,353
|
|||||
|
|
|
|||||
LONG
TERM LIABILITIES
|
|
|
|||||
Deferred
revenue
|
6,127
|
6,767
|
|||||
TOTAL
LIABILITIES
|
954,322
|
743,120
|
|||||
|
|
|
|||||
COMMITMENTS
AND CONTINGENCIES (Note 5)
|
|
|
|||||
|
|
|
|||||
STOCKHOLDERS'
EQUITY
|
|
|
|||||
Preferred
stock; 1,000,000 shares authorized; 0 outstanding
|
-
|
-
|
|||||
Common
stock, $.01 par value; 20,000,000 shares authorized;
|
|
|
|||||
2,192,175
shares issued and outstanding
|
21,922
|
21,922
|
|||||
Additional
paid-in capital
|
6,402,821
|
6,284,616
|
|||||
Retained
(deficit) earnings
|
(1,134,501
|
)
|
206,604
|
||||
Total
stockholders' equity
|
5,290,242
|
6,513,142
|
|||||
TOTAL
LIABILITIES AND STOCKHOLDERS' EQUITY
|
$
|
6,244,564
|
$
|
7,256,262
|
|
The
accompanying notes are an integral part of these consolidated financial
statements
1
CONSOLIDATED
STATEMENTS OF OPERATIONS
(UNAUDITED)
For
the Three Months Ended
|
|||||||
March
31,
|
|||||||
2008
|
2007
|
||||||
REVENUE:
|
|||||||
PCT
Products, services, other
|
$
|
81,473
|
$
|
37,943
|
|||
Grant
revenue
|
50,903
|
93,678
|
|||||
Total
revenue
|
132,376
|
131,621
|
|||||
COSTS
AND EXPENSES:
|
|||||||
Cost
of PCT products and services
|
48,449
|
31,654
|
|||||
Research
and development
|
490,931
|
461,532
|
|||||
Selling
and marketing
|
463,161
|
256,530
|
|||||
General
and administrative
|
501,248
|
481,082
|
|||||
Total
operating costs and expenses
|
1,503,789
|
1,230,798
|
|||||
Operating
loss from continuing operations
|
(1,371,413
|
)
|
(1,099,177
|
)
|
|||
OTHER
INCOME:
|
|||||||
Realized
gain on securities available for sale
|
-
|
727,473
|
|||||
Interest
income
|
30,308
|
71,602
|
|||||
Total
other income
|
30,308
|
799,075
|
|||||
Loss
before income taxes
|
(1,341,105
|
)
|
(300,102
|
)
|
|||
Income
taxes from continuing operations
|
-
|
40,519
|
|||||
Loss
from continuing operations
|
(1,341,105
|
)
|
(259,583
|
)
|
|||
DISCONTINUED
OPERATIONS:
|
|||||||
Loss
on discontinued operations
|
-
|
(378,503
|
)
|
||||
Net
loss
|
$
|
(1,341,105
|
)
|
$
|
(638,086
|
)
|
|
Loss
per share from continuing operations - basic and
diluted
|
$
|
(0.61
|
)
|
$
|
(0.13
|
)
|
|
Loss
per share from discontinued operations - basic and
diluted
|
-
|
(0.18
|
)
|
||||
Net
loss per share - basic and diluted
|
$
|
(0.61
|
)
|
$
|
(0.31
|
)
|
|
Weighted
average number of shares used to calculate loss per share - basic
and
diluted
|
2,192,175
|
2,065,425
|
The
accompanying notes are an integral part of these consolidated financial
statements
2
CONSOLIDATED
STATEMENTS OF COMPREHENSIVE LOSS
(UNAUDITED
)
For
the Three Months Ended
|
|||||||
March
31,
|
|||||||
2008
|
2007
|
||||||
Net
loss
|
$
|
(1,341,105
|
)
|
$
|
(638,086
|
)
|
|
Holding
gain
|
-
|
302,146
|
|||||
Reclassification
of unrealized gain to realized gain on securities during the
period
|
-
|
(727,473
|
)
|
||||
Unrealized
loss on marketable securities
|
-
|
(425,327
|
)
|
||||
Income
tax benefit related to items of
|
|||||||
other
comprehensive loss
|
-
|
122,910
|
|||||
Total
other comprehensive loss, net of taxes
|
-
|
(302,417
|
)
|
||||
Comprehensive
loss
|
$
|
(1,341,105
|
)
|
$
|
(940,503
|
)
|
The
accompanying notes are an integral part of these consolidated financial
statements
3
PRESSURE
BIOSCIENCES, INC. AND SUBSIDIARIES
CONSOLIDATED
STATEMENTS OF CASH FLOWS
(UNAUDITED)
For
the Three Months Ended
|
|||||||
March
31,
|
|||||||
2008
|
2007
|
||||||
CASH
FLOWS FROM OPERATING ACTIVITIES:
|
|||||||
Net
loss
|
$
|
(1,341,105
|
)
|
$
|
(638,086
|
)
|
|
Adjustments
to reconcile loss to net cash used in operating
activities:
|
|||||||
Depreciation
and amortization
|
41,004
|
35,478
|
|||||
Non-cash,
stock-based compensation expense
|
118,205
|
111,757
|
|||||
Realized
gain on sale of marketable securities
|
-
|
(727,473
|
)
|
||||
Changes
in operating assets and liabilities:
|
|||||||
Accounts
receivable
|
11,604
|
(93,611
|
)
|
||||
Inventories
|
(422,512
|
)
|
(50,202
|
)
|
|||
Deposits
|
341,922
|
(176,000
|
)
|
||||
Income
tax receivable and prepaid taxes
|
(230
|
)
|
(51,319
|
)
|
|||
Prepaid
expenses and other current assets
|
(125,624
|
)
|
(50,183
|
)
|
|||
Accounts
payable
|
225,880
|
122,077
|
|||||
Accrued
employee compensation
|
(13,046
|
)
|
(72,369
|
)
|
|||
Deferred
revenue and other accrued expenses
|
(3,002
|
)
|
13,543
|
||||
Net
cash used in operating activities from continuing
operations
|
(1,166,904
|
)
|
(1,576,388
|
)
|
|||
CASH
FLOWS FROM INVESTING ACTIVITIES:
|
|||||||
Additions
to property and equipment
|
(110,762
|
)
|
(29,679
|
)
|
|||
Proceeds
from sale of marketable securities
|
-
|
728,938
|
|||||
Net
cash (used in) provided by investing activities from continuing
operations
|
(110,762
|
)
|
699,259
|
||||
CASH
FLOWS FROM DISCONTINUED OPERATIONS:
|
|||||||
Cash
flows from operating activities
|
-
|
378,503
|
|||||
Net
cash provided by discontinued operations
|
-
|
378,503
|
|||||
CHANGE
IN CASH AND CASH EQUIVALENTS:
|
(1,277,666
|
)
|
(498,626
|
)
|
|||
Cash
and cash equivalents, beginning of period
|
5,424,486
|
5,335,282
|
|||||
Cash
and cash equivalents, end of period
|
$
|
4,146,820
|
$
|
4,836,656
|
|||
SUPPLEMENTAL
INFORMATION:
|
|||||||
Income
taxes paid
|
$
|
2,790
|
$
|
10,800
|
|||
Income
taxes received
|
834
|
-
|
The
accompanying notes are an integral part of these consolidated financial
statements
4
PRESSURE
BIOSCIENCES, INC.
NOTES
TO CONSOLIDATED FINANCIAL STATEMENTS
AS
OF MARCH 31, 2008
1)
|
Business
Overview and Management
Plans
|
We
are a
life sciences company focused on the development and commercialization of
a
novel, enabling, platform technology called pressure cycling technology (“PCT”).
PCT uses cycles of hydrostatic pressure between ambient and ultra-high levels
(up to 35,000 psi and greater) to control bio-molecular
interactions.
Our
pressure cycling technology uses internally developed instrumentation that
is
capable of cycling pressure between ambient and ultra-high levels at controlled
temperatures to rapidly and repeatedly control the interactions of
bio-molecules. Our instrument, the Barocycler®, and our internally developed
consumables product line, which includes PULSE (Pressure Used to Lyse Samples
for Extraction) Tubes as well as the ProteoSolve–lrs kit for the detergent-free
extraction of proteins from lipid-rich samples, together make up the PCT
Sample
Preparation System (“PCT SPS”).
We
have
experienced negative cash flows from operations with respect to our pressure
cycling technology business since its inception. As of March 31, 2008, we
had
available cash of approximately $4.1 million. We believe that we have
sufficient liquidity to fund our operations at their current level, and with
planned increases in selected areas of our business, into early 2009. The
extent
to which we increase our operational costs is dependent upon our judgment
of the
investment required to successfully commercialize PCT and our ability to
secure
additional funding through equity or debt financings. If we are unable to
increase the number of installations of Barocycler instruments and if we
are
unable to secure additional funding through equity or debt financings, we
will
be prepared to reduce our spending. We have developed plans based on these
contingencies and such reductions of spending will include the delay of certain
research and development projects and the reduction of the cost of our
workforce. We believe that implementing such changes to our business plan
will
allow us to extend our existing cash balances into the middle of 2009, without
significantly impacting our short-term commercialization efforts.
2)
|
Interim
Financial Reporting
|
The
accompanying unaudited consolidated financial statements of Pressure
BioSciences, Inc. have been prepared in accordance with accounting principles
generally accepted in the United States of America (“generally accepted
accounting principles” or “GAAP”) for interim financial information and with the
instructions to the Quarterly Report on Form 10-Q. Accordingly, they do not
include all of the information and footnotes required by generally accepted
accounting principles for complete financial statements. In the opinion of
management, all adjustments (consisting of only normal recurring adjustments)
considered necessary for a fair presentation have been included. Operating
results for the three months ended March 31, 2008 are not necessarily indicative
of the results that may be expected for the year ending December 31, 2008.
For
further information, refer to the audited consolidated financial statements
and
footnotes thereto included in the Company’s Annual Report on Form 10-K (the
“Form 10-K”) for the fiscal year ended December 31, 2007.
3)
|
Summary
of Significant Accounting
Policies
|
Principles
of Consolidation
The
consolidated financial statements include the accounts of Pressure BioSciences,
Inc., and its wholly-owned subsidiary PBI BioSeq, Inc.
Use
of Estimates
To
prepare our consolidated financial statements in conformity with generally
accepted accounting principles, we are required to make significant estimates
and assumptions that affect the reported amounts of assets and liabilities
and
disclosure of contingent assets and liabilities at the date of the financial
statements and the reported amounts of revenues and expenses during the
reporting period. In addition, significant estimates were made in projecting
future cash flows to quantify impairment of assets, deferred tax assets and
the
costs associated with fulfilling our warranty obligations for the instruments
that we sell, and in our calculation of fair value of stock options awarded.
We
base our estimates on historical experience and on various other assumptions
that we believe to be reasonable under the circumstances, the results of
which
form the basis for making judgments about the carrying values of assets and
liabilities that are not readily apparent from other sources. Actual results
could differ from the estimates and assumptions used.
5
PRESSURE
BIOSCIENCES, INC.
NOTES
TO CONSOLIDATED FINANCIAL STATEMENTS
AS
OF MARCH 31, 2008
Revenue
Recognition
We
recognize revenue in accordance with the Securities and Exchange Commission’s
(“SEC”) Staff Accounting Bulletin (“SAB”) No. 104, Revenue
Recognition
("SAB
104"). Revenue is recognized when realized or earned when all the following
criteria have been met: persuasive evidence of an arrangement exists; delivery
has occurred and risk of loss has passed to the customer; the seller’s price to
the buyer is fixed or determinable; and collectibility is reasonably
assured.
Our
current instruments, the Barocycler NEP3229 and NEP2320, require a basic
level
of instrumentation expertise to set-up for initial operation. To support
a
favorable first experience for our customers, we send a representative to
the
customer site to install every Barocycler that we sell through our domestic
sales force. The installation process includes uncrating and setting up the
instrument and conducting an introductory user training course. Product revenue
related to current Barocycler instrumentation is recognized upon the
installation of our instrumentation at the customer location. Product revenue
related to sales of PCT products to our foreign distributors is recognized
upon
shipment through a common carrier. We provide for the expected costs of warranty
upon the recognition of revenue for the sales of our instrumentation. Our
sales
arrangements do not provide our customers with a right of return. Product
revenue related to our consumable products such as PULSE Tubes and
ProteoSolve-lrs kits is recorded upon shipment through a common carrier.
Shipping costs are included in the costs of sales. Any shipping costs
billed to customers are recognized as revenue.
In
accordance with the Financial Accounting Standards Board (“FASB”) Statement of
Financial Accounting Standards (“SFAS”) No. 13, “Accounting
for Leases”,
we
account for our lease agreements under the operating method. We record revenue
over the life of the lease term and we record depreciation expense on a
straight-line basis over the thirty-six month estimated useful life of the
Barocycler instrument. Many of our lease and rental agreements allow the
lessee
to purchase the instrument at any point during the term of the agreement
with
partial credit for rental payments previously
made. The depreciation expense associated with assets under lease agreement
is
included in the “Cost of PCT products and services” line item in our
Consolidated Statements of Operations. We pay all maintenance costs associated
with the instrument during the term of the leases.
Revenue
from government grants is recorded when expenses are incurred under the grant
in
accordance with the terms of the grant award.
Our
transactions sometimes involve multiple elements (i.e., products and services).
Revenue under multiple element arrangements is recognized in accordance with
Emerging Issues Task Force (“EITF”) Issue No. 00-21, “Accounting
for Revenue Arrangements with Multiple Deliverables”.
Under
this method, if an element is determined to be a separate unit of accounting,
the revenue for the element is based on fair value and determined by vendor
specific objective evidence (“VSOE”), and recognized at the time of delivery. If
an arrangement includes undelivered elements that are not essential to the
functionality of the delivered elements, we defer the fair value of the
undelivered elements with the residual revenue allocated to the delivered
elements. Fair value is determined based upon the price charged when the
element
is sold separately. If there is not sufficient evidence of the fair value
of the
undelivered elements, no revenue is allocated to the delivered elements and
the
total consideration received is deferred until delivery of those elements
for
which objective and reliable evidence of the fair value is not available.
We
provide certain customers with extended service contracts and, to the extent
VSOE is established, these service revenues are recognized ratably over the
life
of the contract which is generally one to four years.
Cash
and Cash Equivalents
Our
policy is to invest available cash in short-term, investment grade
interest-bearing obligations, including money market funds, and bank and
corporate debt instruments. Securities purchased with initial maturities
of
three months or less are valued at cost plus accrued interest, which
approximates fair market value, and are classified as cash equivalents.
Research
and Development
Research
and development costs, which are comprised of costs incurred in performing
research and development activities including wages and associated employee
benefits, facilities, consumable products and overhead costs that are expensed
as incurred. Our research activities are performed at our laboratories in
Woburn, Massachusetts and Rockville, Maryland and in conjunction with the
collaboration partner sites. In support of our research and development
activities we utilize our Barocycler instruments that are capitalized as
fixed
assets and depreciated over their expected useful life.
6
PRESSURE
BIOSCIENCES, INC.
NOTES
TO CONSOLIDATED FINANCIAL STATEMENTS
AS
OF MARCH 31, 2008
Inventories
Inventories
are valued at the lower of cost or market. The composition of inventory as
of March 31, 2008 and December 31, 2007 is as follows:
March
31,
|
December
31,
|
||||||
2008
|
2007
|
||||||
Raw
materials
|
$
|
44,615
|
$
|
28,115
|
|||
Finished
goods
|
550,445
|
144,433
|
|||||
Total
|
$
|
595,060
|
$
|
172,548
|
Property
and Equipment
Property
and equipment are stated at cost, less accumulated depreciation. For financial
reporting purposes, depreciation is recognized using the straight-line method,
allocating the cost of the assets over their estimated useful lives of three
years for certain laboratory equipment, from three to five years for management
information systems and office equipment, and three years for all PCT finished
units classified as fixed assets.
Intangible
Assets
We
have
classified as intangible assets, costs associated with the fair value of
acquired intellectual property. Intangible assets including patents are
being amortized on a straight-line basis over sixteen years. We perform a
quarterly review of our intangible assets for impairment. When impairment
is indicated, any excess of carrying value over fair value is recorded as
a
loss. An impairment analysis of intangible assets was performed as of December
31, 2007 and was reviewed as of March 31, 2008. We have concluded that no
impairment of intangible assets had occurred.
Long-Lived
Assets and Deferred Costs
In
accordance with the FASB SFAS No. 144, “Accounting
for the Impairment or Disposal of Long-Lived Assets”
, if
indicators of impairment exist, we assess the recoverability of the affected
long-lived assets by determining whether the carrying value of such assets
can
be recovered through the undiscounted future operating cash flows. If impairment
is indicated, we measure the amount of such impairment by comparing the carrying
value of the asset to the fair value of the asset and record the impairment
as a
reduction in the carrying value of the related asset and a charge to operating
results. While our current and historical operating losses and cash flow
are
indicators of impairment, we performed an impairment analysis at December
31,
2007 and reviewed the analysis as of March 31, 2008 and determined that
such long-lived assets were not impaired.
Concentrations
Credit
Risk
Our
financial instruments that potentially subject us to concentrations of credit
risk consist primarily of cash, cash equivalents and trade receivables. We
have
cash investment policies which, among other things, limit investments to
investment-grade securities. We perform ongoing credit evaluations of our
customers, and the risk with respect to trade receivables is further mitigated
by the fact that many of our customers are government institutions and
university labs.
During
the three months ended March 31, 2008 and 2007 our top five customers accounted
for 84.2% and approximately 100% of our total revenues, respectively. During
the
three months ended March 31, 2008 and 2007, various agencies of the Federal
Government of the United States in the aggregate accounted for 39.5% and
73.7%
of our total revenues, respectively.
As
of
March 31, 2008 and December 31, 2007 our top five accounts receivable accounted
for 96.9% and 93.8% of our total receivables balance, respectively. As of
March
31, 2008 and December 31, 2007, various agencies of the Federal Government
of
the United States in the aggregate accounted for 47.6% and 40.9% of our total
accounts receivable, respectively.
Product
Supply
Source
Scientific, LLC has been our sole contract manufacturer for all of our PCT
instrumentation. We have initiated several engineering initiatives to position
us for greater independence from any one supplier, and we are in the process
of
developing a network of manufacturers and sub-contractors to reduce our reliance
on any single supplier. Until we develop a broader network of manufacturers
and
subcontractors, obtaining alternative sources of supply or manufacturing
services could involve significant delays and other costs and challenges,
and
may not be available to us on reasonable terms, if at all. The failure of
a
supplier or contract manufacturer to provide sufficient quantities, acceptable
quality and timely products at an acceptable price, or an interruption of
supplies from such a supplier could harm our business and prospects.
7
PRESSURE
BIOSCIENCES, INC.
NOTES
TO CONSOLIDATED FINANCIAL STATEMENTS
AS
OF MARCH 31, 2008
Computation
of Loss per Share
Basic
loss per share is computed by dividing loss available to common shareholders
by
the weighted average number of common shares outstanding. Diluted loss per
share
is computed by dividing loss available to common shareholders by the weighted
average number of common shares outstanding plus additional common shares
that
would have been outstanding if dilutive potential common
shares
had been issued. For purposes of this calculation, stock options are considered
common stock equivalents in periods in which they have a dilutive effect.
Stock
options that are anti-dilutive are excluded from this calculation. The following
table illustrates our computation of loss per share for the three months
ended
March 31, 2008 and 2007.
For
the Three Months Ended
|
|||||||
March
31,
|
|||||||
2008
|
2007
|
||||||
Numerator:
|
|||||||
Loss
from continuing operations - basic and diluted
|
$
|
(1,341,105
|
)
|
$
|
(259,583
|
)
|
|
Denominator:
|
|||||||
Weighted
Average Shares Outstanding - basic and diluted
|
2,192,175
|
2,065,425
|
|||||
Loss
per share from continuing operations - basic and diluted
|
$
|
(0.61
|
)
|
$
|
(0.13
|
)
|
|
Shares
excluded from calculations
|
196,785
|
101,089
|
Accounting
for Income Taxes
Effective
January 1, 2007, we adopted the provisions of FASB Interpretation
No. 48, “Accounting for
Uncertainty in Income Taxes - an Interpretation of FASB Statement
No. 109”“FIN
48”). FIN
48
clarifies the accounting for uncertainty in income taxes recognized in an
enterprise’s financial statements in accordance with SFAS No. 109,
“Accounting
for Income Taxes”.
This
interpretation prescribes a recognition threshold and measurement attribute
for
the financial statement recognition and measurement of a tax position taken
or
expected to be taken in a tax return. FIN 48 also provides guidance on
de-recognition of tax benefits, classification on the balance sheet, interest
and penalties, accounting in interim periods, disclosure, and transition.
We
account for income taxes under the asset and liability method, which requires
recognition of deferred tax assets, subject to valuation allowances, and
liabilities for the expected future tax consequences of events that have
been
included in the financial statements or tax returns. Deferred income taxes
reflect the net tax effects of temporary differences between the carrying
amounts of asset and liabilities for financial reporting and income tax
purposes. A valuation allowance is established if it is more likely than
not
that all or a portion of the net deferred tax assets will not be realized.
Accounting
for Stock-Based Compensation
We
maintain equity compensation plans under which grants of incentive stock
options
and non-qualified stock options are granted to employees, independent members
of
our Board of Directors and outside consultants. We recognize equity compensation
expense over the requisite service period using the Black-Sholes formula
to
estimate the fair value of the stock options on the date of grant. Since
January
1, 2006, we have accounted for our stock option expense in accordance with
the
provisions of SFAS No. 123 (revised 2004), “Share-Based
Payment”,
or SFAS
123R.
We
recognized stock-based compensation expense of $118,205 and $111,757 for
the
three months ended March 31, 2008 and 2007, respectively. The following table
summarizes the effect of this stock-based compensation expense within each
of
the line items of our costs and expenses within our Consolidated Statement
of
Operations:
8
PRESSURE
BIOSCIENCES, INC.
NOTES
TO CONSOLIDATED FINANCIAL STATEMENTS
AS
OF MARCH 31, 2008
For
the Three Months Ended, March 31,
|
|||||||
2008
|
2007
|
||||||
Cost
of PCT products and services
|
$
|
-
|
$
|
2,620
|
|||
Research
and development
|
43,237
|
49,494
|
|||||
Selling
and marketing
|
33,032
|
15,995
|
|||||
General
and administrative
|
41,936
|
43,648
|
|||||
Total
stock-based compensation expense
|
$
|
118,205
|
$
|
111,757
|
The
provisions of SFAS 123R require that we make an estimate of our forfeiture
rate
and adjust the expense that we recognize to reflect the estimated number
of
stock options that will go unexercised. Our historical forfeiture rate has
been
approximately 5%, so we used this historical rate as our assumption in
calculating future stock-based compensation expense.
During
the three months ended March 31, 2008 and 2007, the total fair value of stock
options awarded was $127,552 and $267,805, respectively.
As
of
March 31, 2008, the total estimated fair value of unvested stock options
to be
amortized over their remaining vesting period was $666,921. The non-cash,
stock
based compensation expense associated with the vesting of these options will
be
$333,251 in 2008, $238,311 in 2009, $90,750 in 2010 and $4,609 in 2011.
Fair
Value of Financial Instruments
Due
to
their short maturities, the carrying amounts for cash and cash equivalents,
accounts receivable, accounts payable, and accrued expenses approximate their
fair value. Long-term liabilities are primarily related to liabilities
transferred under contractual arrangements with carrying values that approximate
fair value.
Reclassifications
Investment
in Marketable Securities
As
of
March 31, 2008 we held 0 shares of common stock of Panacos Pharmaceuticals,
Inc.
During the three months ended March 31, 2007 we sold 161,000 shares to generate
a realized gain of $727,473, on proceeds of $728,938. During 2007 we accounted
for this investment in accordance with the provisions of SFAS 115 “Accounting
for Certain Investments in Debt and Equity Securities”
as
securities available for sale.
Advertising
Advertising
costs are expensed as incurred. During the three months ended March 31, 2008
and
2007, we incurred $6,517 and $0, respectively in advertising expense.
Rent
Expense
Rental
costs are expensed as incurred. During the three months ended March 31, 2008
and
2007, we incurred $32,213 and $20,520, respectively in rent expense for the
use
of our corporate office and research and development facilities.
4)
|
Discontinued
Operations
|
In
June 2004, we transferred certain assets and liabilities of our PBI Source
Scientific, Inc. subsidiary to a newly formed limited liability company
known as Source Scientific, LLC. At the time of the transfer, we owned 100%
of
the ownership interests of Source Scientific, LLC. We subsequently sold 70%
of
our ownership interests of Source Scientific, LLC to Mr. Richard Henson and
Mr. Bruce A. Sargeant pursuant to a purchase agreement (the “Source
Scientific Agreement”). As a result of the sale of 70% of our ownership
interests, Mr. Henson and Mr. Sargeant each owned 35% and we owned the
remaining 30% of Source Scientific, LLC. Under the Source Scientific Agreement,
we received notes receivable in the aggregate amount of $900,000 (the “Notes”)
payable at the end of three years bearing 8% interest. The Source Scientific
Agreement offered Mr. Henson and Mr. Sargeant the option (“the
Option”) to purchase our 30% ownership interest in Source Scientific, LLC until
May 31, 2007, at an escalating premium (10-50%) over our initial ownership
value, provided that they first paid off the Notes in their
entirety.
9
PRESSURE
BIOSCIENCES, INC.
NOTES
TO CONSOLIDATED FINANCIAL STATEMENTS
AS
OF MARCH 31, 2008
On
May
29, 2007, we executed a consent agreement with Mr. Henson and Mr. Sargeant,
Source Scientific LLC, and BIT Analytical Instruments, Inc. (“the Consent
Agreement”) pursuant to which the Notes were repaid in full in the aggregate
amount of $1,201,534 in principal and interest, and Mr. Henson and Mr. Sargeant
exercised their Option (through BIT Analytical Instruments, Inc.) to purchase
our remaining 30% ownership interest in Source Scientific, LLC for an aggregate
price of $578,573. As a result of these transactions we no longer retain
any
direct or indirect ownership interest in Source Scientific, LLC.
During
the three months ended March 31, 2007, Source Scientific, LLC reported a
net
loss of approximately $483,000. In accordance with the SAB Topic 5E we recorded
a charge in our Consolidated Statements of Operations equal to the net book
value on our Consolidated Balance Sheet of $378,503. Upon execution of the
Consent Agreement we accounted for the total gain on the sale of our ownership
interests in Source Scientific, LLC as discontinued operations. The charge
that
we recorded during the first quarter of 2007 has been reclassified to reflect
this change.
5)
|
Commitments
and Contingencies
|
Operating
Leases
Our
corporate offices are currently located at 14 Norfolk Avenue, South Easton,
Massachusetts 02375. In November 2007, we signed an 18 month lease
agreement commencing in February 2008, pursuant to which we lease approximately
5,500 square feet of office space, with an option for an additional 18 months.
We pay approximately $6,500 per month for the use of these facilities.
On
June
1, 2006, we entered into a lease agreement with Scheer Partners and the Maryland
Economic Development Corporation, pursuant to which we lease laboratory and
office space in Rockville, MD. In August 2007, we extended this lease agreement
through May 31, 2009. We pay approximately $3,300 per month for the use of
these
facilities.
On
March
1, 2006, we entered into a sub-lease agreement with Proteome Systems, pursuant
to which we lease approximately 650 square feet of laboratory space plus
100
square feet of office space from Proteome Systems in Woburn, Massachusetts.
The
lease period extends through December 31, 2008 and we pay approximately $3,200
per month for the use of these facilities.
Royalty
Commitments
In
1996,
we acquired our initial equity interest in BioSeq, Inc., which at the time
was
developing our original pressure cycling technology. BioSeq, Inc. acquired
its pressure cycling technology from BioMolecular Assays, Inc. under a
technology transfer and patent assignment agreement. In 1998, we purchased
all of the remaining outstanding capital stock of BioSeq, Inc., and at such
time, the technology transfer and patent assignment agreement was amended
to
require us to pay BioMolecular Assays, Inc. a 5% royalty on our sales of
products or services that incorporate or utilize the original pressure cycling
technology that BioSeq, Inc. acquired from BioMolecular Assays, Inc. We
are also required to pay BioMolecular Assays, Inc. 5% of the proceeds from
any
sale, transfer or license of all or any portion of the original pressure
cycling
technology. These payment obligations terminate in 2016. During the
three months ended March 31, 2008 and 2007, we incurred approximately $3,000
and
$2,000, respectively in royalty expense associated with our obligation to
BMA
Laboratories.
In
connection with our acquisition of BioSeq, Inc., we licensed certain limited
rights to the original pressure cycling technology back to BioMolecular Assays,
Inc. This license is non-exclusive and limits the use of the
original pressure cycling technology by BioMolecular Assays, Inc. solely
for
molecular applications in scientific research and development and in scientific
plant research and development. BioMolecular Assays, Inc. is required to
pay us a royalty equal to 20% of any license or other fees and royalties,
but
not including research support and similar payments, it receives in connection
with any sale, assignment, license or other transfer of any rights granted
to
BioMolecular Assays, Inc. under the license. BioMolecular Assays, Inc. must
pay
us these royalties until the expiration of the patents held by BioSeq, Inc.
in
1998, which we anticipate will be 2016. We have not received any royalty
payments from BioMolecular Assays, Inc. under this license.
Purchase
Commitments
In
March
2007, we executed a purchase order with Source Scientific, LLC under which
we
agreed to purchase 20 Barocycler NEP3229 units and nine demonstration (NEP2320)
units to be used by our sales force. In connection with this purchase order,
we
placed deposits with Source Scientific, LLC in the amount of $260,000. The
nine
demonstration (NEP2320) instruments were prototype units and were therefore
billable on a time and materials basis. As of December 31, 2007 we took
possession of all of these prototype NEP2320 units and the cost was expensed
as
incurred as research and development expense within our Consolidated Statements
of Operations. The order for 20 NEP3229 units is based on a fixed bill of
materials and we are billed for the complete cost of each unit as it is
completed, net of the deposit we placed for each instrument. As of March
31,
2008, 16 of the NEP3229’s had been completed. We expect the remaining 4 units to
be completed and available for sale, lease or collaboration in the second
quarter of 2008.
10
PRESSURE
BIOSCIENCES, INC.
NOTES
TO CONSOLIDATED FINANCIAL STATEMENTS
AS
OF MARCH 31, 2008
In
June
2007, we executed a purchase order with Source Scientific, LLC under which
we
agreed to purchase 40 Barocycler NEP2320 units. In connection with this purchase
order we placed a deposit with Source Scientific, LLC in the amount of $140,000.
In accordance with the terms of this purchase order, we are billed based
on a
fixed bill of materials, for the complete cost of each unit as it is completed,
net of the deposit we placed for each instrument.
As
of
March 31, 2008, we had $87,000 on deposit with Source for 14 remaining units
pursuant to these purchase orders. As of December 31, 2007 we had $379,000
on
deposit with Source for 54 remaining units pursuant to open purchase orders.
Indemnification
In
connection with our sale of substantially all of the assets of Boston Biomedica,
Inc. (“BBI Core Businesses”) to SeraCare Life Sciences, Inc. in September 2004,
we continue to be exposed to possible indemnification claims in amounts up
to
the purchase price of approximately $29 million. Our indemnification obligations
for breaches of some representations and warranties relating to compliance
with
environmental laws extend until September 14, 2009, representations and
warranties relating to tax matters extend for the applicable statute of
limitations period (which varies depending on the nature of claim), and
representations and warranties relating to our due organization, subsidiaries,
authorization to enter into and perform the transactions contemplated by
the
Asset Purchase Agreement and brokers fees, extend indefinitely.
Severance
and Change of Control Agreements
Each
of
our executive officers, Mr. Schumacher, Mr. Myles, Dr. Ting, Dr. Lazarev,
Dr.
Lawrence, and Mr. Potter, is entitled to receive a severance payment if
terminated by the Company without cause. The severance benefits would include
a
payment in an amount equal to one year of each executive officer’s annualized
base salary compensation plus accrued paid time off. Additionally, each
executive officer will be entitled to receive medical and dental insurance
coverage for one year following the date of termination. The total commitment
related to these agreements in the aggregate is approximately $1.2 million.
Each
of
our executive officers, other than Mr. Schumacher, is entitled to receive
a
change of control payment in an amount equal to one year of such executive
officer’s annualized base salary compensation, accrued paid time off, and
medical and dental coverage, in the event of a change of control of the Company.
In the case of Mr. Schumacher, this payment would be equal to two years of
annualized base salary compensation, accrued paid time off, and two years
of
medical and dental coverage. The total commitment related to these agreements
in
the aggregate is approximately $1.5 million.
6)
|
Stockholders’
Equity
|
Preferred
Stock
In
1996,
our Board of Directors authorized the issuance of 1,000,000 shares of preferred
stock with a par value of $0.01. As of March 31, 2008 none of these shares
have
been issued.
Shareholders
Rights Plan
On
March
3, 2003, our Board of Directors adopted a shareholder rights plan (“the Rights
Plan”) and declared a distribution of one Right for each outstanding share of
our Common Stock to shareholders of record at the close of business on March
21,
2003 (the “Rights”). Initially, the Rights will trade automatically with the
common stock and separate Right Certificates will not be issued. The
Rights Plan is designed to deter coercive or unfair takeover tactics and
to
ensure that all of our shareholders receive fair and equal treatment in the
event of an unsolicited attempt to acquire the Company. The Rights Plan was
not
adopted in response to any effort to acquire the Company and the Board is
not
aware of any such effort. The Rights will expire on February 27, 2013 unless
earlier redeemed or exchanged. Each Right entitles the registered holder,
subject to the terms of a Rights Agreement, to purchase from the Company
one
one-thousandth of a share of the Company’s Series A Junior Participating
Preferred Stock at a purchase price of $45.00 per one one-thousandth of a
share,
subject to adjustment. In general, the Rights will not be exercisable until
a
subsequent distribution date which will only occur if a person or group acquires
beneficial ownership of 15% or more of our common stock or announces a tender
or
exchange offer that would result in such person or group owning 15% or more
of
the common stock. With respect to any person or group who currently beneficially
owns 15% or more of our common stock, the Rights will not become exercisable
unless and until such person or group acquires beneficial ownership of
additional shares of common stock.
11
PRESSURE
BIOSCIENCES, INC.
NOTES
TO CONSOLIDATED FINANCIAL STATEMENTS
AS
OF MARCH 31, 2008
Subject
to certain limited exceptions, if a person or group acquires beneficial
ownership of 15% or more of our outstanding common stock or if a current
15%
beneficial owner acquires additional shares of common stock, each holder
of a
Right (other than the 15% holder whose Rights become void once such holder
reaches the 15% threshold) will thereafter have a right to purchase, upon
payment of the purchase price of the Right, that number of shares of our
common
stock which at the time of such transaction will have a market value equal
to
two times the purchase price of the Right. In the event that, at any time
after a person or group acquires 15% or more of our common stock, we are
acquired in a merger or other business combination transaction or 50% or
more of
our consolidated assets or earning power are sold, each holder of a Right
will
thereafter have the right to purchase, upon payment of the purchase price
of the
Right, that number of shares of common stock of the acquiring company which
at
the time of such transaction will have a market value of two times the purchase
price of the Right.
Our
Board
of Directors may exchange the Rights (other than Rights owned by such person
or
group which have become void), in whole or in part, at an exchange ratio
of one
share of common stock per Right (subject to adjustment). At any time prior
to the time any person or group acquires 15% or more of our Common Stock,
the
Board of Directors may redeem the Rights in whole, but not in part, at a
price
of $0.001 per Right.
Stock
Options
On
June
16, 2005, our stockholders approved our 2005 Equity Incentive Plan (the “Plan”)
pursuant to which an aggregate of 1,000,000 shares of our common stock were
reserved for issuance upon exercise of stock options or other equity awards
made
under the Plan. Under the Plan, we may award stock options, shares of
common stock, and other equity interests in the Company to employees, officers,
directors, consultants, and advisors, and to any other persons the Board
of
Directors deems appropriate. As of March 31, 2008, options to acquire 914,000
shares were outstanding under the Plan.
We
also
have 244,000 stock options outstanding under our 1999 Non-qualified Plan
and
9,500 stock options outstanding under our 1994 Incentive Stock Option Plan.
As
of March 31, 2008, there were 4,800 shares available for future grant under
the
1999 Non-qualified Plan. The 1994 Incentive Stock Option Plan expired;
therefore, there are no shares available for future grants under this
plan.
The
following tables summarize information concerning options outstanding and
exercisable:
Stock
Options
|
|
||||||||||||
|
|
|
Weighted
|
Weighted
|
|||||||||
Average
price
|
Average
price
|
||||||||||||
Shares
|
per
share
|
Exercisable
|
per
share
|
||||||||||
Balance
outstanding, 12/31/2007
|
1,120,500
|
$
|
3.45
|
691,166
|
$
|
3.23
|
|||||||
Granted
|
47,000
|
4.36
|
|||||||||||
Exercised
|
-
|
||||||||||||
Expired
|
-
|
||||||||||||
Forfeited
|
-
|
||||||||||||
Balance
outstanding, 3/31/2008
|
1,167,500
|
$
|
3.49
|
754,166
|
$
|
3.27
|
|
Options
Outstanding
|
Options
Exercisable
|
|||||||||||||||||
Weighted
Average
|
Weighted
Average
|
||||||||||||||||||
Range
of Exercise Prices
|
Number
of Options
|
Remaining
Contractual Life
|
Exercise
Price
|
Number
of Options
|
Remaining
Contractual Life
|
Exercise
Price
|
|||||||||||||
$2.50
-
$2.70
|
159,000
|
4.4
|
$
|
2.64
|
159,000
|
4.4
|
$
|
2.64
|
|||||||||||
2.71
-
3.08
|
343,000
|
6.4
|
2.96
|
276,333
|
6.2
|
2.97
|
|||||||||||||
3.09
-
3.95
|
389,500
|
8.1
|
3.71
|
191,833
|
7.9
|
3.71
|
|||||||||||||
3.96
-
5.93
|
276,000
|
8.7
|
4.32
|
127,000
|
7.6
|
4.05
|
|||||||||||||
$2.50
-
$5.93
|
1,167,500
|
7.2
|
$
|
3.49
|
754,166
|
6.5
|
$
|
3.27
|
The
aggregate intrinsic value of options outstanding and exercisable as of March
31,
2008 and December 31, 2007 is illustrated in the table below:
12
PRESSURE
BIOSCIENCES, INC.
NOTES
TO CONSOLIDATED FINANCIAL STATEMENTS
AS
OF MARCH 31, 2008
March
31, 2008
|
December
31, 2007
|
||||||
Stock
options, outstanding
|
$
|
361,925
|
$
|
2,162,565
|
|||
Stock
options, exercisable
|
399,708
|
1,486,007
|
Stock
Buy-back Program
During
the quarter ended September 30, 2006 our Board of Directors approved a stock
buy-back program pursuant to which we are authorized to use up to $500,000
of
our cash resources to purchase shares of the Company’s common stock in the open
market or in privately negotiated transactions. We did not acquire any shares
through our stock buy-back program during the three months ended March 31,
2008
and 2007.
Sale
of Common Stock
On
November 21, 2007, we completed a private placement pursuant to which we
sold an
aggregate of 126,750 shares of common stock, $0.01 par value (the “Shares”), for
a purchase price of $5.00 per share, resulting in gross proceeds to us of
approximately $633,750 (the “Private Placement”). The Shares were issued and
sold to a total of 8 accredited investors pursuant to a Securities Purchase
Agreement entered into as of November 21, 2007 (the “Securities Purchase
Agreement”).
The
Shares were issued in the Private Placement without registration under the
Securities Act of 1933, as amended (the “Securities Act”), in reliance upon the
exemption from registration set forth in Rule 506 of Regulation D (“Regulation
D”) promulgated under the Securities Act. We based such reliance upon
representations made by each purchaser of Shares, including, but not limited
to,
representations as to the purchaser’s status as an “accredited investor” (as
defined in Rule 501(a) under Regulation D) and the purchaser’s investment
intent. The Shares were not offered or sold by any form of general solicitation
or general advertising, as such terms are used in Rule 502 under Regulation
D.
The Shares may not be offered or sold in the United States absent an effective
registration statement or an exemption from the registration requirements
under
applicable federal and state securities laws.
In
connection with the Private Placement, we agreed to prepare and file a
Registration Statement on Form S-3 (the “Registration Statement”) covering the
resale of the Shares purchased in the Private Placement, and to use our
commercially reasonable efforts to cause such Registration Statement to be
declared effective as promptly as possible after the filing thereof and to
keep
the Registration Statement continuously effective under the Securities Act
until
all shares covered by such Registration Statement have been sold, or may
be sold
without volume restrictions pursuant to Rule 144 (or any successor Rule under
the Securities Act). The Registration Statement was declared effective by
the
SEC on January 22, 2008.
13
SPECIAL
NOTE REGARDING FORWARD-LOOKING STATEMENTS
This
Quarterly Report on Form 10-Q contains forward-looking statements within
the
meaning of Section 27A of the Securities Act of 1933 and Section 21E of the
Securities Exchange Act of 1934. In some cases, forward-looking statements
are identified by terms such as “may”, “will”, “should”, “could”, “would”,
“expects”, “plans”, “anticipates”, “believes”, “estimates”, “projects”,
“predicts”, “potential”, and similar expressions intended to identify
forward-looking statements. Such statements include, without limitation,
statements regarding:
|
-
|
our
plans and expectations with respect to our pressure cycling technology
(PCT) operations;
|
|
-
|
potential
growth in the market for our PCT products;
|
|
-
|
market
acceptance and the potential for commercial success of our PCT
products;
|
|
-
|
our
belief that PCT provides a superior solution for sample
preparation;
|
-
|
the
expected development and success of new product
offerings;
|
|
|
-
|
the
potential applications for PCT;
|
-
|
the
expected benefits and results from our research and development
efforts;
|
|
-
|
the
expected benefits and results from our collaboration
program;
|
|
|
-
|
our
belief that we have sufficient liquidity to finance operations
into early
2009;
|
-
|
our
expectation of obtaining additional research grants from the government
in
the future;
|
|
|
-
|
the
amount of cash necessary to operate our business;
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our
ability to raise additional capital when needed;
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the
availability of net operating losses to offset potential future
operating
income;
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general
economic conditions; and
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the
anticipated future financial performance and business operations
of our
company.
|
These
forward-looking statements are only predictions and involve known and unknown
risks, uncertainties, and other factors that may cause our actual results,
levels of activity, performance, or achievements to be materially different
from
any future results, levels of activity, performance, or achievements expressed
or implied by such forward-looking statements. Also, these forward-looking
statements represent our estimates and assumptions only as of the date of
this
Report. Except as otherwise required by law, we expressly disclaim any
obligation or undertaking to release publicly any updates or revisions to
any
forward-looking statement contained in this Report to reflect any change
in our
expectations or any change in events, conditions, or circumstances on which
any
of our forward-looking statements are based or to conform to actual
results. Factors that could cause or contribute to differences in our
future financial and operating results include those discussed in the risk
factors set forth in Item 6 of our Annual Report on Form 10-K for the year
ended
December 31, 2007, as well as those discussed elsewhere in this Report. We
qualify all of our forward-looking statements by these cautionary
statements.
You
should read this section in combination with the section entitled Management’s
Discussion and Analysis of Financial Condition and Results of Operations
for the
year ended December 31, 2007 included in our Annual Report on Form 10-K for
the year ended December 31, 2007.
14
OVERVIEW
We
are a
life sciences company focused on the development and commercialization of
a
novel, enabling, platform technology called pressure cycling technology (“PCT”).
PCT uses cycles of hydrostatic pressure between ambient and ultra-high levels
(up to 35,000 psi and greater) to control bio-molecular
interactions.
Our
pressure cycling technology uses internally developed instrumentation that
is
capable of cycling pressure between ambient and ultra-high levels at controlled
temperatures to rapidly and repeatedly control the interactions of
bio-molecules. Our instrument, the Barolcycler®, and our internally developed
consumables product line, which includes PULSE (Pressure Used to Lyse Samples
for Extraction) Tubes as well as the ProteoSolve-lrs kit
for
the detergent-free extraction of proteins from lipid-rich samples, together
make
up the PCT Sample Preparation System (“PCT SPS”).
Our
pressure cycling technology employs a unique approach that we believe has
the
potential for broad applications in a number of established and emerging
life
sciences areas, including;
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|
sample
preparation for genomic, proteomic, and small molecule
studies;
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pathogen
inactivation;
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protein
purification;
|
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|
control
of chemical (enzymatic) reactions; and
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immunodiagnostics.
|
Since
we
began operations as Pressure BioSciences in February 2005, we have focused
substantially all of our research and development and commercialization efforts
on sample preparation for genomic, proteomic, and small molecule
studies.
Our
business strategy is to commercialize pressure cycling technology in the
area of
sample preparation for genomic, proteomic, and small molecule studies (“sample
preparation”). We also plan to pursue the further development and
commercialization of PCT in other life sciences applications, which could
include working with various strategic partners that have greater scientific
and
regulatory expertise in the respective applications than we do.
To
support our current strategy, our primary focus in 2007 and the first quarter
of
2008 was the execution of our commercialization plan for PCT in sample
preparation. We increased our spending in important areas of our business
during
2007 and 2008, including increased expenses associated with additional staff
in
the areas of sales and research and development to support our sales expansion
and increased research and development activities.
If
we are
successful commercializing our technology in the sample preparation market,
we
believe that our financial results will be positively affected by a combination
of the revenue from the sale, lease, and rental of the Barocycler instruments,
and by the recurring revenue streams that we hope to realize from the sale
of
the single-use PULSE Tubes, PCT-dependent kits (such as ProteoSolve-lrs),
and extended
service contracts on our instrumentation. We believe the recurring revenue
streams that could be generated from our instruments in the field is a very
important component of our future financial success. Therefore, we believe
that
in the short-term it is more important for us to focus on increasing the
number
of installed Barocyclers in the field than it is for us to record revenue
in the
current period. To this end, we have offered our prospective customers the
opportunity to lease or rent the Barocycler instruments. While these
arrangements do not provide us with the immediate revenue of a sale, they
do
serve to expand the utilization of PCT and they provide a stream of revenue
from
the monthly rental income and the sale of consumable products. We define
sales,
leases, and rentals of Barocycler instruments as revenue-generating
installations.
We
also
derive revenue from Small Business Innovation Research (“SBIR”) grants awarded
to us by the National Institutes of Health. In September 2006, and in March
2007, we received SBIR Phase I grants in the aggregate amount of $300,000.
These
grants have funded experiments to demonstrate the feasibility of using pressure
cycling technology in various applications in the life sciences. If our work
in
SBIR Phase I grants is successful, then we expect to have the opportunity
to
apply for larger NIH SBIR Phase II grants. We have several SBIR Phase I and
II
grants under review at the present time. Additionally, if our work with the
SBIR
grants is successful, the publication of Application Notes in specific areas
of
research should further support our commercialization efforts.
15
RESULTS
OF OPERATIONS
Three
Months Ended March 31, 2008 and 2007
Revenue
We
recognized revenue of $132,376 for the three months ended March 31, 2008,
as
compared to $131,621 for the same period in the prior year.
Revenue
from the sale of PCT products and services was $81,473 for the three months
ended March 31, 2008 as compared to $37,943 for the same period in the prior
year. During the first quarter of 2008 we completed the installation of seven
Barocycler instruments at customer locations, as compared to one in the same
period of 2007. Also contributing to the increase in revenue was an increase
in
the number of PULSE Tubes and ProteoSolve-lrs kits sold. During the first
quarter of 2008, four of our installations were completed pursuant to the
terms
of lease and rental agreements and three were outright sales.
We
expect
the number of units installed will continue to increase in future periods
as we
continue to commercialize our technology. We also expect that some portion
of
future installations will be for the smaller, lower priced, Barocycler NEP2320
model and some will be placed under lease or short-term rental agreements.
Therefore, the average revenue per installation may fluctuate from period
to
period as we continue to drive our installed base and commercialize
PCT.
During
the three months ended March 31, 2008 and 2007, we recorded $50,903 and $93,678
of grant revenue, respectively, in connection with our two SBIR Phase 1 grants.
This decrease in grant revenue was due to a shift in resources from grant
related activities to other research and development projects.
Cost
of PCT Products and Services
The
cost
of PCT products and services was $48,449 for the three months ended March
31,
2008 compared to $31,654 for the comparable period in 2007. This decrease
in
overall cost of goods sold as a percentage of revenue is due primarily to
a
shift in the product mix to include an increasing number of consumables and
the
sale of a Barocycler NEP2320 unit, which has a higher gross margin than the
NEP3229.
We
believe that our cost of PCT products and services will continue to improve
as a
percentage of revenue as we continue to install more instrumentation, and
sell
more consumable products, such as PULSE Tubes and ProteoSolve-lrs kits. However,
we expect our gross margin may fluctuate from period to period as we continue
to
sell, lease, or rent a varying mix of Barocycler instrumentation.
Research
and Development
Research
and development expenditures increased to $490,931 in the first quarter of
2008
as compared to $461,532 in the same period in 2007. This increase in research
and development expense was due primarily to the planned expansion of our
research and development staff and an increase in the number of scientific
projects our staff is managing within our own laboratories. This increase
in
headcount and project spending is consistent with our strategy to continue
to
evaluate and potentially offer new applications of PCT within the life sciences’
sample preparation field.
Research
and development expense recognized in the first quarter of 2008 and 2007
included $43,237 and $49,494, respectively, of non-cash, stock-based
compensation expense. We expect the level of stock-based compensation expense
for the remaining quarters of 2008 to be similar to the first quarter.
We
plan
to reduce the level of hiring in 2008, relative to 2007. Therefore, we expect
our spending in this area to increase less significantly than it has in prior
periods. We believe that with our existing staff, we can continue to pursue
research and development programs, and continue to invest successfully in
our
intellectual property portfolio, in the sample preparation area.
Selling
and Marketing
Selling
and marketing expenses increased to $463,161 for the three months ended March
31, 2008 from $256,530 for the comparable period in 2007. This increase was
the
result of our growth from two selling and marketing employees in the first
quarter of 2007 to nine in the first quarter of 2008.
16
During
the first quarter of 2008 and 2007, selling and marketing expense included
$33,032 and $15,995, respectively, of non-cash, stock-based compensation
expense. We expect the level of stock-based compensation expense for the
remaining quarters of 2008 to be similar to the first quarter.
We
expect
selling and marketing expense for the remaining quarters of 2008 to continue
to
increase relative to the expense incurred during the first quarter as we
continue to develop and train our domestic sales force and expand our foreign
distribution network. Additionally, we plan to continue our expansion of
our
marketing programs for the remainder of 2008 in order to drive toward successful
commercialization of PCT.
General
and Administrative
General
and administrative costs totaled $501,248 for the three months ended March
31,
2008, as compared to $481,082 for the comparable period in 2007. The increase
in
general and administrative costs is due to increased spending in connection
with
Sarbanes-Oxley compliance, and our investor relations program.
Our
general and administrative costs for the first quarter of 2008 included $41,936
of stock-based compensation expense as compared to $43,648 in the first quarter
of 2007. We expect that the level of stock-based compensation expense to
be
recorded in the second quarter of 2008 will increase due to the expense
associated with the award of 10,000 non-qualified, fully-vested stock options
to
each of the four independent members of our Board of Directors.
We
expect
that general and administrative spending, excluding stock-based compensation
expense for the full year of 2008, to be approximately the same as it was
in
2007. We will continue to incur costs in support of our investor relations
programs, Sarbanes-Oxley compliance, and other requirements associated with
being a publicly-traded company, and continued investment in the development
of
our infrastructure.
Operating
Loss from Continuing Operations
Our
operating loss from continuing operations was $1,371,413 for the three months
ended March 31, 2008 as compared to an operating loss from continuing operations
of $1,099,177 for the comparable period in 2007. The increase in operating
loss
from continuing operations was primarily the result of the planned increases
in
activities within our research and development and selling and marketing
functions of our business.
The
operating loss from continuing operations for the three months ended March
31,
2008 included $118,205 of non-cash, stock-based compensation expense as compared
to $111,757 in the comparable period in 2007.
We
expect
our operating loss in 2008 to be higher than the operating loss incurred
in
2007, due primarily to expected increased spending in our sales and marketing
activities and, to a lesser extent, our research and development activities.
We
do, however, expect that the gross profit from increasing revenues will
partially mitigate the impact of our increased spending on our overall operating
loss.
Realized
gain of sale on securities held for sale
In
the
three months ended March 31, 2007 we sold 161,000 shares of Panacos
Pharmaceuticals and realized a gain on securities sold of $727,473. We completed
the liquidation of our investment in Panacos Pharmaceuticals during the second
quarter of 2007.
Interest
Income
Interest
income totaled $30,308 for the three months ended March 31, 2008 as compared
to
interest income of $71,602 in the prior year period. The decrease is due
to
lower average cash balances and lower yields on these balances during 2008,
as
compared to 2007.
Income
Taxes from Continuing Operations
In
the
quarter ended March 31, 2008, we did not record a benefit for income taxes
from
continuing operations. During the same period in 2007, we recorded a benefit
for
income taxes of $40,519.
We
do not
expect to record any income tax benefit for the foreseeable future due to
the
fact that we are no longer able to carry back current losses against taxable
income from prior periods and because we expect our operating losses to continue
for several years. If we are successful commercializing PCT and if we are
able
to generate operating income, then we may be able to utilize the net operating
loss carry-forwards that we generate.
17
Gain
on Assets Related to Discontinued Operations
During
the first half of 2007, we realized a gain on the sale of Source Scientific,
LLC
of $1,155,973. This gain is comprised of the $378,503 charge that we recorded
in
the first quarter of 2007 under the provisions of Staff Accounting Bulletin
(“SAB”) Topic 5E, “Accounting
for Divestiture of a Subsidiary or Other Business Operation
(“SAB
Topic 5E”) and the gain of $1,534,476, net of income taxes of $218,060, that we
recorded during the second quarter of 2007, the period in which we completed
the
sale. We recorded this gain in connection with the receipt on May 29, 2007
of
$1,780,071 from Mr. Richard W. Henson and Mr. Bruce A. Sargeant, the principals
of Source Scientific, LLC, as full payment for their purchase of our remaining
interest in that business.
Upon
completion of the transaction, we accounted for the total gain on the sale
of
our ownership interests in Source Scientific, LLC as discontinued operations.
The charge that we recorded during the first quarter of 2007, under the
provisions of SAB Topic 5E, has been reclassified as discontinued operations
to
reflect this change.
Net
loss
During
the first quarter of 2008 we recorded a net loss of $1,341,105 as compared
to a
net loss of $638,086 in the first quarter of 2007. Our increase in net loss
is
the result of increased operating costs in 2008 relative to 2007 in all areas
of
our operations, most notably in our selling and marketing activities.
Additionally, although we expect our revenue to increase, our net loss in
2008
will not be mitigated by the gain on sale of marketable securities, gain
on sale
of assets from discontinued operations, and the benefit from income taxes,
as
was the case in 2007. We therefore expect our net loss for the full year
of 2008
to be higher than the net loss reported for the full year in 2007
LIQUIDITY
AND FINANCIAL CONDITION
As
of
March 31, 2008, our working capital position was $4,640,524, the primary
components of which were cash and cash equivalents, accounts receivable,
inventory, prepaid expenses, deposits, and income taxes receivable, partially
offset by accounts payable, accrued employee compensation, and other accrued
expenses. As of December 31, 2007, our working capital balance was $5,933,822,
the primary components of which were cash and cash equivalents, income taxes
receivable, prepaid expenses, and deposits. We expect to continue to fund
our
operations from our working capital balance. We believe that we have sufficient
cash and working capital to fund our operations into early 2009.
Net
cash
used in continuing operations for the three months ended March 31, 2008 was
$1,166,904 as compared to net cash used in continuing operations of $1,576,388
for the three months ended March 31, 2007.
Net
cash
used by investing activities for the three months ended March 31, 2008 was
$110,762 as compared to cash provided of $699,259 for the same period in
the
prior year. The cash used in the first three months of 2008 was the result
of
the purchase of furniture and fixtures associated with our move to new corporate
offices. The cash generated in the same period in 2007 was entirely from
the
sale of 161,000 shares of Panacos common stock, partially offset by purchases
of
fixed assets.
There
were no cash flows from discontinued operations during the three months of
2008.
During the three months ended March 31, 2007, Source Scientific, LLC reported
a
net loss of approximately $483,000. In accordance with SAB Topic 5E we recorded
a charge in our Consolidated Statements of Operations equal to the net book
value on our Consolidated Balance Sheet of $378,503. In connection with the
sale
of our remaining 30% ownership interest in Source Scientific, LLC at the
end of
May 2007, we accounted for the total gain on the sale of our ownership interests
in Source Scientific, LLC as discontinued operations. The charge that we
recorded during the first quarter of 2007 has been reclassified to reflect
this
change.
COMMITMENTS
AND CONTINGENCIES
Operating
Leases
Our
corporate offices are currently located at 14 Norfolk Avenue, South Easton,
Massachusetts 02375. In November 2007, we signed an 18 month lease
agreement commencing in February 2008, pursuant to which we lease approximately
5,500 square feet of office space, with an option for an additional 18 months.
We pay approximately $6,500 per month for the use of these facilities.
On
June
1, 2006, we entered into a lease agreement with Scheer Partners and the Maryland
Economic Development Corporation, pursuant to which we lease laboratory and
office space in Rockville, MD. In August 2007, we extended this lease agreement
through May 31, 2009. We pay approximately $3,300 per month for the use of
these
facilities.
18
On
March
1, 2006, we entered into a sub-lease agreement with Proteome Systems, pursuant
to which we lease approximately 650 square feet of laboratory space plus
100
square feet of office space from Proteome Systems in Woburn, Massachusetts.
The
lease period extends through December 31, 2008 and we pay approximately $3,200
per month for the use of these facilities.
Royalty
Commitments
In
1996,
we acquired our initial equity interest in BioSeq, Inc., which at the time
was
developing our original pressure cycling technology. BioSeq, Inc. acquired
its pressure cycling technology from BioMolecular Assays, Inc. under a
technology transfer and patent assignment agreement. In 1998, we purchased
all of the remaining outstanding capital stock of BioSeq, Inc., and at such
time, the technology transfer and patent assignment agreement was amended
to
require us to pay BioMolecular Assays, Inc. a 5% royalty on our sales of
products or services that incorporate or utilize the original pressure cycling
technology that BioSeq, Inc. acquired from BioMolecular Assays, Inc. We
are also required to pay BioMolecular Assays, Inc. 5% of the proceeds from
any
sale, transfer or license of all or any portion of the original pressure
cycling
technology. These payment obligations terminate in 2016. During the
three months ended March 31, 2008 and 2007, we incurred approximately $3,000
and
$2,000, respectively in royalty expense associated with our obligation to
BMA
Laboratories.
In
connection with our acquisition of BioSeq, Inc., we licensed certain limited
rights to the original pressure cycling technology back to BioMolecular Assays,
Inc. This license is non-exclusive and limits the use of the
original pressure cycling technology by BioMolecular Assays, Inc. solely
for
molecular applications in scientific research and development and in scientific
plant research and development. BioMolecular Assays, Inc. is required to
pay us a royalty equal to 20% of any license or other fees and royalties,
but
not including research support and similar payments, it receives in connection
with any sale, assignment, license or other transfer of any rights granted
to
BioMolecular Assays, Inc. under the license. BioMolecular Assays, Inc. must
pay
us these royalties until the expiration of the patents held by BioSeq, Inc.
in
1998, which we anticipate will be 2016. We have not received any royalty
payments from BioMolecular Assays, Inc. under this license.
Purchase
Commitments
In
March
2007, we executed a purchase order with Source Scientific, LLC under which
we
agreed to purchase 20 Barocycler NEP3229 units and nine demonstration (NEP2320)
units to be used by our sales force. In connection with this purchase order,
we
placed deposits with Source Scientific, LLC in the amount of $260,000. The
nine
demonstration (NEP2320) instruments were prototype units and were therefore
billable on a time and materials basis. As of December 31, 2007 we took
possession of all of these prototype NEP2320 units and the cost was expensed
as
incurred as research and development expense within our Consolidated Statements
of Operations. The order for 20 NEP3229 units is based on a fixed bill of
materials and we are billed for the complete cost of each unit as it is
completed, net of the deposit we placed for each instrument. As of March
31,
2008, 16 of the NEP3229’s had been completed. We expect the remaining 4 units to
be completed and available for sale, lease or collaboration in the second
quarter of 2008.
In
June
2007, we executed a purchase order with Source Scientific, LLC under which
we
agreed to purchase 40 Barocycler NEP2320 units. In connection with this purchase
order we placed a deposit with Source Scientific, LLC in the amount of $140,000.
In accordance with the terms of this purchase order, we are billed based
on a
fixed bill of materials, for the complete cost of each unit as it is completed,
net of the deposit we placed for each instrument.
As
of
March 31, 2008, we had $87,000 on deposit with Source for 14 remaining units
pursuant to these purchase orders. As of December 31, 2007 we had $379,000
on
deposit with Source for 54 remaining units pursuant to open purchase orders.
Indemnification
In
connection with our sale of substantially all of the assets of Boston Biomedica,
Inc. (“BBI Core Businesses”) to SeraCare Life Sciences, Inc. in September 2004,
we continue to be exposed to possible indemnification claims in amounts up
to
the purchase price of approximately $29 million. Our indemnification obligations
for breaches of some representations and warranties relating to compliance
with
environmental laws extend until September 14, 2009, representations and
warranties relating to tax matters extend for the applicable statute of
limitations period (which varies depending on the nature of claim), and
representations and warranties relating to our due organization, subsidiaries,
authorization to enter into and perform the transactions contemplated by
the
Asset Purchase Agreement, and brokers fees, extend indefinitely.
19
Severance
and Change of Control Agreements
Each
of
our executive officers, Mr. Schumacher, Mr. Myles, Dr. Ting, Dr. Lazarev,
Dr.
Lawrence, and Mr. Potter, is entitled to receive a severance payment if
terminated by the Company without cause. The severance benefits would include
a
payment in an amount equal to one year of each executive officer’s annualized
base salary compensation plus accrued paid time off. Additionally, each
executive officer will be entitled to receive medical and dental insurance
coverage for one year following the date of termination. The total commitment
related to these agreements in the aggregate is approximately $1.2 million.
Each
of
our executive officers, other than Mr. Schumacher, is entitled to receive
a
change of control payment in an amount equal to one year of such executive
officer’s annualized base salary compensation, accrued paid time off, and
medical and dental coverage, in the event of a change of control of the Company.
In the case of Mr. Schumacher, this payment would be equal to two years of
annualized base salary compensation, accrued paid time off, and two years
of
medical and dental coverage. The total commitment related to these agreements
in
the aggregate is approximately $1.5 million.
RECENT
ACCOUNTING STANDARDS
In
September 2006, the FASB issued Statement of Financial Accounting Standards
No. 157, “Fair Value Measurements”, (“SFAS 157”). SFAS 157 defines fair
value, establishes a framework for measuring the fair value of assets and
liabilities, and expands disclosure requirements regarding the fair value
measurement. SFAS 157 does not expand the use of fair value measurements.
This
statement, as issued, is effective for financial statements issued for fiscal
years beginning after November 15, 2007, and interim periods within those
fiscal years. FASB Staff Position (FSP) FAS No. 157-2 was issued in February
2008 and deferred the effective date of SFAS 157 for nonfinancial assets
and
liabilities to fiscal years beginning after November 2008. As such, the Company
adopted SFAS 157 as of January 1, 2008 for financial assets and liabilities
only. There was no significant effect on the Company’s financial statements. As
of March 31, 2008, the Company’s financial assets subject to SFAS 157 consisted
of held to maturity investments in marketable securities and investments
in
non-publicly traded companies; financial liabilities consisted of derivatives
for forward contracts. The Company determined fair value for the investments
in
marketable securities and the derivative liabilities based on quoted market
prices in active markets (i.e. Level 1 as defined under SFAS 157); fair value
for investments in non-publicly traded companies was based on third party
valuation models (i.e. Level 2 as defined under SFAS 157). The Company does
not
believe that the adoption of SFAS 157 to non-financial assets and liabilities
will significantly effect its financial statements.
In
December 2007, the FASB issued SFAS 141 (revised 2007), “Business
Combinations”
(“SFAS
141(R)”) and SFAS No. 160, “Non-controlling
Interests in Consolidated Financial Statements – an amendment of ARB
No. 51”
(“SFAS
160”).
SFAS
141(R) significantly changes the accounting for business combinations. Under
SFAS 141(R), an acquiring entity will be required to recognize all the assets
acquired and liabilities assumed in a transaction at the acquisition-date
at
fair value with limited exceptions. SFAS 141(R) further changes the accounting
treatment for certain specific items, including:
- |
Acquisition
costs will be generally expensed as incurred;
|
- |
Noncontrolling
interests (formerly known as “minority interests” – see SFAS 160
discussion below) will be valued at fair value at the acquisition
date;
|
- |
Acquired
contingent liabilities will be recorded at fair value at the acquisition
date and subsequently measured at either the higher of such amount
or the
amount determined under existing guidance for non-acquired contingencies;
|
- |
In-process
research and development will be recorded at fair value as an
indefinite-lived intangible asset at the acquisition date;
|
- |
Restructuring
costs associated with a business combination will be generally
expensed
subsequent to the acquisition date; and
|
-
|
Changes
in deferred tax asset valuation allowances and income tax uncertainties
after the acquisition date generally will affect income tax expense.
|
SFAS
141(R) includes a substantial number of new disclosure requirements. SFAS
141(R)
applies prospectively to business combinations for which the acquisition
date is
on or after January 1, 2009.
SFAS
160
establishes new accounting and reporting standards for the non-controlling
interest in a subsidiary and for the deconsolidation of a subsidiary.
Specifically, this statement requires the recognition of non-controlling
interests (minority interests) as equity in the consolidated financial
statements and separate from the parent’s equity. The amount of net income
attributable to non-controlling interests will be included in consolidated
net
income on the face of the income statement. SFAS 160 clarifies that changes
in a
parent’s ownership interest in a subsidiary that does not result in
deconsolidation are treated as equity transactions if the parent retains
its
controlling financial interest. In addition, this statement requires that
a
parent recognize a gain or loss in net income when a subsidiary is
deconsolidated. Such gain or loss will be measured using the fair value of
the
non-controlling equity investment on the deconsolidation date. SFAS 160 also
includes expanded disclosure requirements regarding the interests of the
parent
and its non-controlling interest.
20
SFAS
160
is effective for fiscal years, and interim periods within such year, beginning
January 1, 2009. Early adoption of both SFAS 141(R) and SFAS 160 is
prohibited. We do not expect that either SFAS 141(R) or SFAS 160 will have
a
material affect on our consolidated results of operations and financial
condition.
21
ITEM
4T. CONTROLS AND PROCEDURES
We
maintain disclosure controls and procedures that are designed to ensure that
information required to be disclosed in our Securities Exchange Act of 1934
reports is recorded, processed, summarized and reported within the time periods
specified in the SEC’s rules and forms, and that such information is accumulated
and communicated to our management, including our President and Chief Executive
Officer (Principal Executive Officer) and Chief Financial Officer (Principal
Financial Officer), as appropriate, to allow timely decisions regarding required
disclosure. In designing and evaluating the disclosure controls and procedures,
management recognized that any controls and procedures, no matter how well
designed and operated, can provide only reasonable assurance of achieving
the
desired control objectives, as ours are designed to do, and management
necessarily was required to apply its judgment in evaluating the cost-benefit
relationship of possible controls and procedures.
As
of
March 31, 2008, we carried out an evaluation, under the supervision and with
the
participation of our management, including our President and Chief Executive
Officer (Principal Executive Officer) and Chief Financial Officer (Principal
Financial Officer) of the effectiveness of the design and operation of our
disclosure controls and procedures, as defined in Rules 13a-15(e) and
15d-15(e) under the Securities Exchange Act of 1934. Based upon that evaluation,
our President and Chief Executive Officer (Principal Executive Officer) and
Chief Financial Officer (Principal Financial Officer) concluded that our
disclosure controls and procedures are effective in enabling us to record,
process, summarize, and report information required to be included in our
periodic SEC filings within the required time period and to ensure that
information required to be disclosed in such reports that we file or submit
under the Securities Exchange Act of 1934 is accumulated and communicated
to our
management, including our President and Chief Executive Officer (Principal
Executive Officer) and Chief Financial Officer (Principal Financial Officer)
to
allow timely decisions regarding required disclosure.
There
have been no changes in our internal control over financial reporting that
occurred during the period covered by this Report that have materially affected,
or are reasonably likely to materially affect, our internal control over
financial reporting.
22
None
|
|
Reference
|
||
|
|
|
|
|
31.1
|
Principal
Executive Officer Certification Pursuant to Item 601(b)(31) of
Regulation
S-K, as adopted pursuant to Section 302 of the Sarbanes-Oxley Act
of
2002
|
|
Filed
herewith
|
|
|
|
|
|
|
31.2
|
Principal
Financial Officer Certification Pursuant to Item 601(b)(31) of
Regulation
S-K, as adopted pursuant to Section 302 of the Sarbanes-Oxley Act
of
2002
|
|
Filed
herewith
|
|
|
|
|
|
|
32.1
|
Principal
Executive Officer Certification Pursuant to Item 601(b)(32) of
Regulation
S-K, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act
of
2002
|
|
Filed
herewith
|
|
|
|
|
|
|
32.2
|
Principal
Financial Officer Certification Pursuant to Item 601(b)(32) of
Regulation
S-K, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act
of
2002
|
|
Filed
herewith
|
23
Pursuant
to the requirements of the Securities Exchange Act of 1934, the registrant
caused this report to be signed on its behalf by the undersigned thereunto
duly
authorized.
|
PRESSURE
BIOSCIENCES, INC.
|
|
Date: May
9, 2008
|
By:
|
/s/
Richard
T. Schumacher
|
|
Richard
T. Schumacher
President, Chief Executive Officer & Treasurer (Principal Executive Officer) |
Date:
May 9, 2008
|
By:
|
/s/ Edward
H. Myles
|
|
Edward
H. Myles
Senior Vice President of Finance & Chief Financial Officer (Principal Financial and Accounting Officer) |
24