Adynxx, Inc. - Quarter Report: 2008 September (Form 10-Q)

form10q.htm

SECURITIES AND EXCHANGE COMMISSION

WASHINGTON, D.C. 20549

____________________

FORM 10-Q

(Mark One)

x	QUARTERLY REPORT UNDER SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

For quarterly period ended September 30, 2008

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: 000-29819

____________________

HEPALIFE TECHNOLOGIES, INC.

(Exact name of registrant as specified in its charter)

Florida (State or other jurisdiction of incorporation)		58-2349413 (I.R.S. Employer Identification No.)

60 State Street, Suite 700, Boston, MA (Address of principal executive offices)		02109 (Zip Code)

(800) 518-4879

(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. Yes T No o.

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.

Large accelerated filer o Accelerated filer o

Non-accelerated filer o (Do not check if a smaller reporting company) Smaller reporting company T

Indicate by check mark whether the registrant is a shell company (as defined in 12b-2 of the Exchange Act.) Yes o No T.

Indicate the number of shares outstanding of each of the issuer’s classes of common stock, as of the latest practicable date: 91,596,829 shares of Common Stock, par value $0.001, were outstanding on November 14, 2008.

TABLE OF CONTENTS

HEPALIFE TECHNOLOGIES, INC.

FORM 10-Q, QUARTER ENDED SEPTEMBER 30, 2008

PART I FINANCIAL INFORMATION

Item 1. Financial Statements

Interim Unaudited Consolidated Balance Sheets	3

Interim Unaudited Consolidated Statements of Operations	4

Interim Unaudited Consolidated Statement of Stockholders’ Equity (Deficiency)	5

Interim Unaudited Consolidated Statements of Cash Flows	9

Notes to Interim Consolidated Financial Statements	10

Item 2. Management's Discussion and Analysis of Financial Condition and Results of Operations	18

Item 4. Controls and Procedures	23

PART II OTHER INFORMATION

Item 1. Legal Proceedings	24

Item 2. Unregistered Sales of Equity Securities and Use of Proceeds	24

Item 3. Defaults Upon Senior Securities	24

Item 4. Submission of Matters to a Vote of Security Holders	24

Item 5. Other Information	24

Item 6. Exhibits and Reports on Form 8-K	24

Signatures	25

Table of Contents

Item 1. Financial Statements

HEPALIFE TECHNOLOGIES, INC.
(A Development Stage Company)

CONSOLIDATED BALANCE SHEETS
September 30, 2008 and December 31, 2007
(Unaudited)

	September 30,			December 31,
(Expressed in U.S. Dollars)	2008			2007

ASSETS
Current assets
Cash	$	3,653,554		$	534,113
Prepaid expenses and other receivables		53,689			4,338
Total current assets		3,707,243			538,451

Equipment, net (Note 7)		-			10,882
License fee (Note 5)		75,000			75,000
Deferred financing costs (Note 9)		-			210,728

Total assets	$	3,782,243		$	835,061

LIABILITIES
Current liabilities
Accounts payable and accrued liabilities	$	48,872		$	4,800
Accounts payable - related parties (Note 4)		-			208,330
Notes payable - related party (Note 4)		-			877,800
Total current liabilities		48,872			1,090,930

Convertible promissory note, at face value (Note 9)		-			755,000
Discount on convertible promissory notes (Note 9)		-			(468,343	)
		-			286,657

Total liabilities		48,872			1,377,587

Commitments and Contingencies (Note 5, 6)

STOCKHOLDERS' EQUITY (DEFICIENCY)

Stockholders' Equity (Deficiency)
Preferred stock: $0.10 par value; Authorized: 1,000,000 Issued and outstanding: none		-			-
Common stock: $0.001 par value; Authorized: 300,000,000Issued and outstanding: 91,596,829 (2007: 76,264,584)		91,598			76,265
Additional paid-in capital		21,806,840			15,039,050
Common stock issuable		170,000			-
Accumulated other comprehensive income (loss)		(3,356	)		(3,772	)
Loss accumulated during the development stage		(18,331,711	)		(15,654,069	)

Total stockholders' equity (deficiency)		3,733,371			(542,526	)

Total liabilities and stockholders' equity (deficiency)	$	3,782,243		$	835,061


(The accompanying notes are an integral part of these financial statements)

Table of Contents

HEPALIFE TECHNOLOGIES, INC.
(A Development Stage Company)

CONSOLIDATED STATEMENTS OF OPERATIONS
For the three months and nine months ended September 30, 2008 and 2007
and from inception (October 21, 1997) to September 30, 2008
(Unaudited)
													From inception
													(October 21, 1997)
	Three months ended September 30,						Nine months ended September 30,						to September 30,
(Expressed in U.S. Dollars)	2008			2007			2008			2007			2008

Revenue	$	-		$	-		$	-		$	-		$	-

Expenses
Administrative and general		74,038			67,938			145,408			170,453			786,756
Depreciation		2,607			4,177			7,820			12,078			35,409
Professional fees- accounting and legal		60,783			17,920			149,588			93,385			657,109
Management and consulting fees (Note 4)		6,593			3,685			8,093			27,127			1,010,430
Research and development (Notes 5 and 6)		84,803			2,095			294,008			66,685			1,315,296
Salary and benefits		343,747			301,012			986,497			1,209,091			5,463,467
Shareholder and investor relations		172,125			270,409			341,595			481,790			4,125,984
Stock offering costs		-			-			-			-			1,926,713
Transfer agent and filing		965			-			2,210			4,468			18,227
Travel		13,746			22,018			34,682			60,195			328,281
		759,407			689,254			1,969,901			2,125,272			15,667,672

Operating Loss		(759,407	)		(689,254	)		(1,969,901	)		(2,125,272	)		(15,667,672	)

Other income (expenses)
Interest on promissory note		-			(18,807	)		(41,615	)		(61,625	)		(355,112	)
Interest, bank charges and foreign exchange loss		(786	)		(274	)		(9,959	)		(5,417	)		(34,505	)
Interest income		14,498			15,851			25,964			30,080			115,252
Other income / (loss)		(3,060	)		-			(3,060	)		-			(3,060	)
Amortization of discount on issuance of convertible promissory notes (Note 9)		-			(1,029,527	)		(468,343	)		(1,092,320	)		(2,093,099	)
Amortization of deferred financing costs (Note 9)		-			(36,991	)		(210,728	)		(45,796	)		(293,515	)
		10,652			(1,069,748	)		(707,741	)		(1,175,078	)		(2,664,039	)

Net loss available to common shareholders	$	(748,755	)	$	(1,759,002	)	$	(2,677,642	)	$	(3,300,350	)	$	(18,331,711	)

Loss per share - basic and diluted	$	(0.01	)	$	(0.02	)	$	(0.03	)	$	(0.04	)

Weighted average number of common shares outstanding - basic and diluted		91,735,959			74,156,604			83,923,575			73,539,141


(The accompanying notes are an integral part of these financial statements)

Table of Contents

HEPALIFE TECHNOLOGIES, INC.

(A Development Stage Company)

CONSOLIDATED STATEMENT OF STOCKHOLDERS' EQUITY (DEFICIENCY)
From inception (October 21, 1997) to September 30, 2008
(Unaudited)

								Common		Accumulated		Loss accumulated						Total
	Common Stock				Additional			Stock		other comprehensive		during development			Comprehensive			stockholders'
(Expressed in U.S. Dollars)	Shares		Amount		paid-in capital			Issuable		income		stage			income (loss)			equity (deficiency)

Common stock issued for service rendered at $0.00025 per share, October 21, 1997		12,000,000	$	12,000	$	(9,000	)			$	-	$	-		$	-		$	3,000

Common stock issued for cash at $0.0625 per share during 1997		1,200,000		1,200		73,800					-		-						75,000

Comprehensive income Income from inception (October 21, 1997) to December 31, 1997		-		-		-					-		42			42			42

Total comprehensive income																42

Balance, December 31, 1997		13,200,000		13,200		64,800			-		-		42						78,042

Common stock issued for service rendered at $0.025 per share, December 15, 1998		16,000,000		16,000		384,000							-						400,000

Comprehensive income (loss) Loss, year ended December 31, 1998		-		-		-							(471,988	)		(471,988	)		(471,988	)

Total comprehensive income																(471,988	)

Balance, December 31, 1998		29,200,000		29,200		448,800			-		-		(471,946	)					6,054

Common stock issued for cash at $0.025 per share, March 1999		12,000,000		12,000		288,000							-						300,000

Comprehensive income (loss) Loss, year ended December 31, 1999		-		-		-							(121,045	)		(121,045	)		(121,045	)

Total comprehensive income																(121,045	)

Balance, December 31, 1999		41,200,000		41,200		736,800			-		-		(592,991	)					185,009

Comprehensive income (loss) Loss, year ended December 31, 2000		-		-		-							(80,608	)		(80,608	)		(80,608	)

Total comprehensive income																(80,608	)

Balance, December 31, 2000		41,200,000		41,200		736,800			-		-		(673,599	)					104,401

Conversion of debt to equity at $0.015 per share, July 31, 2001		8,933,332		8,933		125,067							-						134,000

Comprehensive income (loss) Loss, year ended December 31, 2001		-		-		-							(160,364	)		(160,364	)		(160,364	)

Total comprehensive income																(160,364	)

Balance, December 31, 2001		50,133,332		50,133		861,867			-		-		(833,963	)					78,037

Table of Contents

HEPALIFE TECHNOLOGIES, INC.

(A Development Stage Company)

CONSOLIDATED STATEMENT OF STOCKHOLDERS' EQUITY (DEFICIENCY)
From inception (October 21, 1997) to September 30, 2008 (continued)
(Unaudited)

							Common		Accumulated		Loss accumulated						Total
	Common Stock				Additional		Stock		other comprehensive		during development			Comprehensive			stockholders'
(Expressed in U.S. Dollars)	Shares		Amount		paid-in capital		Issuable		income		stage			income (loss)			equity (deficiency)

Common stock issued for services at $0.06 per share, April 23, 2002		10,000		10		590						-						600

Conversion of debt to equity at $0.05 per share, April 26, 2002		2,160,000		2,160		105,840						-						108,000

Common stock issued for investor relations services at $0.05 per share, July 25, 2002		2,390,000		2,390		117,110						-						119,500

Conversion of debt to equity at $0.05 per share, December 18, 2002		1,920,000		1,920		94,080						-						96,000

Comprehensive income (loss) Loss, year ended December 31, 2002		-		-		-						(375,472	)		(375,472	)		(375,472	)

Total comprehensive income															(375,472	)

Balance, December 31, 2002		56,613,332		56,613		1,179,487		-		-		(1,209,435	)					26,665

Common stock issued pursuant to exercise of stock options during the year at between $0.07 to $2.11 per share		282,500		283		398,317						-						398,600

Common stock issued pursuant to exercise of share purchase warrants in November 2003 at $0.025 per share		7,300,000		7,300		175,200						-						182,500

Comprehensive income (loss) Loss, year ended December 31, 2003		-		-		-						(1,102,723	)		(1,102,723	)		(1,102,723	)

Total comprehensive income															(1,102,723	)

Balance, December 31, 2003		64,195,832		64,196		1,753,004		-		-		(2,312,158	)					(494,958	)

Common stock issued pursuant to exercise of stock options during the year between $0.07 to $2.11 per share		1,622,000		1,622		1,339,998						-						1,341,620

Common stock issued pursuant to exercise of share purchase warrants in December 2004 at $0.025 per share		2,000,000		2,000		48,000						-						50,000

Comprehensive income (loss) Loss, year ended December 31, 2004		-		-		-						(1,435,613	)		(1,435,613	)		(1,435,613	)

Total comprehensive income															(1,435,613	)

Balance, December 31, 2004		67,817,832		67,818		3,141,002		-		-		(3,747,771	)					(538,951	)

Common stock issued pursuant to exercise of stock options in March 2005 at $3.10 per share		50,000		50		154,950						-						155,000

Common stock issued pursuant to exercise of stock options in May 2005 at $2.11 per share		45,000		45		94,905						-						94,950

Common stock issued pursuant to exercise of stock options in June 2005 at $2.11 per share		100,000		100		210,900						-						211,000

Common stock issued pursuant to exercise of stock options in October 2005 at $2.11 per share		40,000		40		84,360						-						84,400

Common stock issued pursuant to exercise of stock options in March 2005 at $2.11 per share		50,000		50		105,450						-						105,500

Common stock issued pursuant to exercise of share purchase warrants in March 2005 at $0.025 per share		1,250,000		1,250		30,000						-						31,250

Restricted common stock issued in June 2005pursuant to share purchase agreement		20,000		20		37,580						-						37,600

Restricted common stock issued in July 2005pursuant to share purchase agreement		691,598		692		1,382,504						-						1,383,196

Comprehensive income (loss) Loss, year ended December 31, 2005												(2,813,602	)		(2,813,602	)		(2,813,602	)

Table of Contents

HEPALIFE TECHNOLOGIES, INC.

(A Development Stage Company)

CONSOLIDATED STATEMENT OF STOCKHOLDERS' EQUITY (DEFICIENCY)
From inception (October 21, 1997) to September 30, 2008 (continued)
(Unaudited)

							Common		Accumulated			Loss accumulated						Total
	Common Stock				Additional		Stock		other comprehensive			during development			Comprehensive			stockholders'
(Expressed in U.S. Dollars)	Shares		Amount		paid-in capital		Issuable		income			stage			income (loss)			equity (deficiency)

Total comprehensive income																(2,813,602	)

Balance, December 31, 2005		70,064,430		70,065		5,241,651		-		-			(6,561,373	)					(1,249,657	)

Restricted common stock issued in January 2006 pursuant to share purchase agreement		374,753		375		505,542				-			-						505,917

Common stock issued in the first quarter of 2006 to Fusion Capital for cash		431,381		431		449,569				-			-						450,000

Common stock issued in the second quarter of 2006 to Fusion Capital for cash		416,303		416		329,584				-			-						330,000

Common stock issued in the third quarter of 2006 to Fusion Capital for cash		758,606		759		584,234				-			-						584,993

Common stock issued in the fourth quarter of 2006 to Fusion Capital for cash		548,371		548		354,455				-			-						355,003

Exercise of stock options		175,000		175		12,075				-			-						12,250

Stock based compensation expenses		-		-		2,607,302				-			-						2,607,302

Comprehensive income (loss) Loss, year ended December 31, 2006													(4,654,499	)		(4,654,499	)		(4,654,499	)

Total comprehensive income																(4,654,499	)

Balance, December 31, 2006		72,768,844		72,769		10,084,412		-		-			(11,215,872	)					(1,058,691	)

Common stock issued in the first quarter of 2007 to Fusion Capital for cash		382,000		382		204,619													205,001

Common stock issued in the second quarter of 2007 to Fusion Capital for cash		509,019		509		289,491													290,000

Common stock converted from convertible promissory notes		2,604,721		2,605		1,742,395													1,745,000

Stock based compensation expenses						935,044													935,044

Proceeds allocated to the warrants issued with the convertible notes						497,689													497,689

Warrants issued for the payment of broker's fees						64,990													64,990

Intrinsic value of the beneficial conversion feature of the notes						1,220,410													1,220,410

Comprehensive income (loss) Foreign currency translation adjustment										(3,772	)					(3,772	)		(3,772	)

Loss, year ended December 31, 2007													(4,438,197	)		(4,438,197	)		(4,438,197	)

Total comprehensive income																(4,441,969	)

Table of Contents

HEPALIFE TECHNOLOGIES, INC.

(A Development Stage Company)

CONSOLIDATED STATEMENT OF STOCKHOLDERS' EQUITY (DEFICIENCY)
From inception (October 21, 1997) to September 30, 2008 (continued)
(Unaudited)

							Common		Accumulated			Loss accumulated						Total
	Common Stock				Additional		Stock		other comprehensive			during development			Comprehensive			stockholders'
(Expressed in U.S. Dollars)	Shares		Amount		paid-in capital		Issuable		income			stage			income (loss)			equity (deficiency)

Balance, December 31, 2007		76,264,584		76,265		15,039,050		-		(3,772	)		(15,654,069	)					(542,526	)

Common stock converted from convertible promissory notes in January 2008		2,342,415		2,343		752,657													755,000

Common stock converted from notes in June 2008		2,065,412		2,065		975,680													977,745

Common stock and warrants issued for cash and placement fees at $0.425 per share in May 2008		10,924,418		10,925		4,519,875													4,530,800

Common shares issued for services received in 2008								170,000											170,000

Stock based compensation expenses						519,578													519,578

Comprehensive income (loss)Foreign currency translation adjustment										416						416			416

Loss, nine months ended September 30, 2008													(2,677,642	)		(2,677,642	)		(2,677,642	)

Total comprehensive income															$	(2,677,226	)

Balance, September 30, 2008		91,596,829	$	91,598	$	21,806,840	$	170,000	$	(3,356	)	$	(18,331,711	)				$	3,733,371


(The accompanying notes are an integral part of these financial statements)

Table of Contents

HEPALIFE TECHNOLOGIES, INC.
(A Development Stage Company)

CONSOLIDATED STATEMENTS OF CASH FLOWS
For the nine months ended September 30, 2008 and 2007
and from inception (October 21, 1997) to September 30, 2008
(Unaudited)
							From inception
							(October 21, 1997)
	September 30,			September 30,			to September 30,
(Expressed in U.S. Dollars)	2008			2007			2008

Cash flows from operating activities
Net Loss	$	(2,677,642	)	$	(3,300,350	)	$	(18,331,711	)
Adjustments to reconcile net loss to net cash from operating activities:
Depreciation		7,820			12,078			35,409
Common stock issued for services		170,000			-			1,031,100
Common stock issued as stock offering costs		-			-			1,926,713
Stock based compensation expenses		519,578			787,648			4,061,924
Loss on disposal of equipment		3,060						3,060
Amortization of discount on issuance of convertible promissory notes		468,343			1,092,320			2,093,099
Amortization of deferred financing costs		210,728			45,796			293,515
Change in assets and liabilities:
Decrease (Increase) in prepaid expenses		(49,349	)		3,225			(53,687	)
Increase (Decrease) in accounts payable		44,072			(121,567	)		48,872
Increase (Decrease) in accounts payable - related party		(108,385	)		30,989			99,945
Net cash used in operating activities		(1,411,775	)		(1,449,861	)		(8,791,761	)

Cash flows from investing activities
Purchase of property and equipment		-			(3,878	)		(38,471	)
Increase in license fees		-			-			(75,000	)
Net cash used in investing activities		-			(3,878	)		(113,471	)

Cash flows from financing activities
Proceeds from issuance of common stock		4,530,800			495,001			9,787,867
Proceeds from issuance of convertible notes		-			2,125,000			2,125,000
Repayment of promissory notes		-			(132,200	)		877,800
Cash paid for finders fee		-			(228,525	)		(228,525	)
Net cash provided by financing activities		4,530,800			2,259,276			12,562,142

Increase in cash and cash equivalents		3,119,025			805,537			3,656,910

Effect of foreign exchange rate		416			(3,131	)		(3,356	)

Cash and cash equivalents, beginning of period		534,113			252,887			-
Cash and cash equivalents, end of period	$	3,653,554		$	1,055,293		$	3,653,554


Supplemental disclosure of cash flow information:
Interest paid in cash	$	150,000		$	25,930		$	247,575
Income tax paid in cash	$	-		$	-		$	-

Non-cash Investing and Financing Activities:
Common stock issued for services	$	232,078		$	-		$	1,093,078
Issuance of common stock as stock offering costs	$	-		$	-		$	1,926,713
Issuance of warrants for deferred financing costs	$	-		$	64,990		$	64,990
Conversion of note payable and related interest payable to equity	$	977,745		$			$	977,745
Conversion of debt to equity	$	755,000		$	-		$	2,500,000


(The accompanying notes are an integral part of these financial statements)

Table of Contents

HEPALIFE TECHNOLOGIES, INC. AND SUBSIDIARIES

(A Development Stage Company)

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (UNAUDITED)

SEPTEMBER 30, 2008

(Expressed in US Dollars)

NOTE 1 - BASIS OF PRESENTATION - GOING CONCERN UNCERTAINITIES

The Company is a development stage biotechnology company focused on the identification, development and eventual commercialization of cell-based technologies and products.

The Company has incurred net operating losses since inception. The Company faces all the risks common to companies in their early stages of development, including under capitalization and uncertainty of funding sources, high initial expenditure levels, uncertain revenue streams, and difficulties in managing growth. The Company’s recurring losses raise substantial doubt about its ability to continue as a going concern and may cause it to cease operations. The Company’s financial statements do not reflect any adjustments that might result from the outcome of this uncertainty. The Company expects to incur losses from its business operations and may require additional funding during 2009. The future of the Company hereafter will depend in large part on the Company’s ability to successfully raise capital from external sources to pay for planned expenditures and to fund operations.

To meet these objectives, the Company completed a private placement for gross proceeds of $4,530,800 on May 23, 2008. Management believes that its current and future plans enable it to continue operations through December 31, 2009. These financial statements do not give effect to any adjustments which would be necessary should the Company be unable to continue as a going concern and therefore be required to realize its assets and discharge its liabilities in other than the normal course of business and at amounts different from those reflected in the accompanying financial statements.

The accompanying unaudited interim consolidated financial statements have been prepared in accordance with Form 10-Q instructions and in the opinion of management contains all adjustments (which are of a normal recurring nature) necessary to present fairly the financial position as of September 30, 2008 and December 31, 2007, and the results of operations for three and nine months ended September 30, 2008 and 2007 and cash flows for the nine months ended September 30, 2008 and 2007. These results have been determined on the basis of generally accepted accounting principles and practices in the United States and applied consistently with those used in the preparation of the Company's 2007 Annual Report on Form 10-K.

NOTE 2: ACCOUNTING POLICIES

Principles of Consolidation

The accompanying consolidated financial statements have been prepared on the accrual basis in accordance with accounting principles generally accepted in the United States, and include the accounts of HepaLife Technologies, Inc. and its subsidiaries, Phoenix BioSystems, Inc., HepaLife Technologies Ltd. and HepaLife Biosystems Inc.. Phoenix BioSystems, Inc. was incorporated under the laws of the State of Nevada on June 6, 2006. HepaLife Technologies Ltd. was incorporated on April 11, 2007 in British Columbia, Canada, for the purpose of streamlining business operations in Canada. HepaLife Biosystems Inc., was incorporated in State of Nevada on April 17, 2007 for the purpose of categorizing operations and accounting associated with the Company’s ongoing research and development efforts associated with its patented PICM-19 cell line, artificial liver technologies, and in vitro toxicology testing systems. All significant inter-company transactions and accounts have been eliminated in consolidation.

Use of Estimates

The preparation of financial statements in conformity with generally accepted accounting principles requires management to make 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. Management makes its best estimate of the ultimate outcome for these items based on historical trends and other information available when the financial statements are prepared. Changes in estimates are recognized in accordance with the accounting rules for the estimate, which is typically in the period when new information becomes available to management. Actual results could differ from those estimates.

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Research and Development

Research and development costs are expensed as incurred.

Recent Accounting Pronouncements

In September 2006, the FASB issued SFAS No. 157, “Fair Value Measurements” (SFAS 157), which defines fair value, establishes a framework for measuring fair value, and expands disclosures about fair-value measurements required under other accounting pronouncements. It does not change existing guidance as to whether or not an instrument is carried at fair value. SFAS 157 is effective for financial statements issued for fiscal years beginning after November 15, 2007, and interim periods within those fiscal years. In February 2008, the FASB issued FASB Staff Position No. FAS 157-1 (FSP FAS 157-1), which excludes SFAS No. 13, “Accounting for Leases” and certain other accounting pronouncements that address fair value measurements under SFAS 13, from the scope of SFAS 157. In February 2008, the FASB issued FASB Staff Position No. 157-2 (FSP 157-2), which provides a one-year delayed application of SFAS 157 for nonfinancial assets and liabilities, except for items that are recognized or disclosed at fair value in the financial statements on a recurring basis (at least annually). The Company is required to adopt SFAS 157 as amended by FSP FAS 157-1 and FSP FAS 157-2 on January 1, 2009, the beginning of its fiscal year 2009. The Company does not expect the application of SFAS No. 157 to have a material effect on the Company’s consolidated financial statements.

In October 2008, the FASB issued FASB Staff Position No. FAS 157-3, “Determining the Fair Value of a Financial Asset in a Market That Is Not Active” (FSP 157-3), which clarifies the application of SFAS 157 when the market for a financial asset is inactive. Specifically, FSP 157-3 clarifies how (1) management’s internal assumptions should be considered in measuring fair value when observable data are not present, (2) observable market information from an inactive market should be taken into account, and (3) the use of broker quotes or pricing services should be considered in assessing the relevance of observable and unobservable data to measure fair value. The guidance in FSP 157-3 is effective immediately and will apply to the Company upon adoption of SFAS 157.

In June 2008, the FASB issued Staff Position EITF 03-06-1, “Determining Whether Instruments Granted in Share-Based Payment Transactions Are Participating Securities” (FSP EITF 03-06-1). FSP EITF 03-06-1 provides that unvested share-based payment awards that contain nonforfeitable rights to dividends or dividend equivalents (whether paid or unpaid) are participating securities and shall be included in the computation of earnings per share pursuant to the two-class method in SFAS No. 128, “Earnings per Share”. EITF 03-06-1 did not have any impact on the Company’s consolidated financial statements.

In December 2007, the FASB issued SFAS No. 160, “Noncontrolling Interests in Consolidated Financial Statements, an Amendment of Accounting Research Bulletin No 51” (SFAS 160). SFAS 160 establishes accounting and reporting standards for ownership interests in subsidiaries held by parties other than the parent, changes in a parent’s ownership of a noncontrolling interest, calculation and disclosure of the consolidated net income attributable to the parent and the noncontrolling interest, changes in a parent’s ownership interest while the parent retains its controlling financial interest and fair value measurement of any retained noncontrolling equity investment. SFAS 160 is effective for financial statements issued for fiscal years beginning after December 15, 2008, and interim periods within those fiscal years. Early adoption is prohibited. The Company must adopt SFAS 160 on January 1, 2009, the beginning of its fiscal year 2009. The Company does not expect the application of SFAS No. 160 to have a material effect on the consolidated financial statements.

In December 2007, the FASB issued SFAS No. 141R, “Business Combinations” (SFAS 141R), which establishes principles and requirements for the reporting entity in a business combination, including recognition and measurement in the financial statements of the identifiable assets acquired, the liabilities assumed, and any noncontrolling interest in the acquiree. SFAS 141R applies prospectively to business combinations for which the acquisition date is on or after the beginning of the first annual reporting period beginning on or after December 15, 2008, and interim periods within those fiscal years. The Company must adopt SFAS 141R on January 1, 2009, the beginning of its fiscal year 2009. The Company does not expect the application of SFAS 141R to have a material effect on the consolidated financial statements.

NOTE 3 - LOSS PER SHARE

Basic earnings or loss per share is based on the weighted average number of common shares outstanding. Diluted earnings or loss per share is based on the weighted average number of common shares outstanding and dilutive common stock equivalents. The computation of earnings (loss) per share is net loss available to common stockholders (numerator) divided by the weighted average number of common shares outstanding (denominator) during the periods presented. All earnings or loss per share amounts in the financial statements are basic earnings or loss per share, as defined by SFAS No. 128, “Earnings Per Share.” Diluted loss per share does not differ materially from basic loss per share for all periods presented. Convertible securities that could potentially dilute basic loss per share in the future are warrants, stock options, and convertible debt are not included in the computation of diluted loss per share because to do so would be anti-dilutive. All per share and per share information are adjusted retroactively to reflect stock splits and changes in par value, when applicable.

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	Three months ended						Nine months ended
	September 30,						September 30,
	2008			2007			2008			2007

Numerator - net loss available to common stockholders	$	(748,755	)	$	(1,759,001	)	$	(2,677,642	)	$	(3,300,350	)

Denominator - weighted average number of common shares outstanding		91,735,959			74,156,604			83,923,575			73,539,141

Basic and diluted loss per common share	$	(0.01	)	$	(0.02	)	$	(0.03	)	$	(0.04	)

NOTE 4 - RELATED PARTY TRANSACTIONS

Management Fees: During the three months and nine months ended September 30, 2008, the Company paid management fees of $6,593 (2007: $685) and $8,093 (2007: $4,150) to the directors respectively. There is no documented management or consulting agreement in effect between the Company and its non-employee board members.

On May 23, 2008, the Company reached an agreement with Mr. Rayat to which Mr. Rayat (i) converted the entire outstanding principal amount ($877,800) of his loan (the “Loan”) to the Company into an aggregate of 2,065,412 Units (at a conversion price of $.425 Unit), each Unit consisting of one share of the Company’s common stock and one Series C Warrant, and (ii) agreed to accept $150,000 in full payment and satisfaction of the accrued and unpaid interest on the Loan in the amount of $249,945.

Rent: Until August 31, 2008, the Company’s administrative office was located at 1628 West 1st Avenue, Suite 216, Vancouver, British Columbia, Canada, V6J 1G1. This premise is owned by a private corporation controlled by a former director and majority shareholder. The Company paid rent of $7,796 (2007: $9,097) and $26,866 (2007: $25,952) for the three months and nine months ended September 30, 2008. Effective September 1, 2008, the Company closed its administrative office in Vancouver, British Columbia, Canada, terminating all of its employees. There were no severance arrangements with any of the terminated employees.

All related party transactions are recorded at the exchange amount established and agreed to between related parties and are in the normal course of business.

NOTE 5 - COOPERATIVE AGREEMENTS

On November 20, 2007, HepaLife Technologies, Inc. entered into a new Cooperative Research and Development Agreement (the “CRADA”) with the U.S. Department of Agriculture (“USDA”), Agricultural Research Service (“ARS”) pertaining to the continued development and use of patented liver cell lines in artificial liver devices and in-vitro toxicological testing platforms, and committed a total payment of $519,130 plus certain expense reimbursements and equipment purchases to USDA-ARS over the two year period, ending November 19, 2009.

As of September 30, 2008, total payments of $542,690 have been paid, including $53,963 for purchases of equipment.

NOTE 6 - LICENSE AGREEMENT

On June 15, 2006, the Company, through its subsidiary, Phoenix BioSystems, Inc. (“PBS”), entered into an exclusive worldwide license agreement with Michigan State University (“MSU”) for the development of new cell-culture based flu vaccines to protect against the spread of influenza viruses among humans, including potentially the high pathogenicity H5N1 virus.

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The license agreement gives the Company exclusive rights to five issued patents. Under the terms of the license agreement, the Company agreed to pay MSU an initial fee of $1,000 (paid) upon execution of the license agreement. A 2.5% annual royalty based on future sales is payable, with an annual minimum payment of $10,000 from 2010 to 2014 and $20,000 from 2015 until the expiration of the last to expire of the patents, or until fifteen (15) years after the effective date of June 15, 2006, whichever is longer.

The Company also has to make milestone payments of $1,000, $2,000, $2,000 and $10,000 to MSU when MSU achieves each of the 4 different developmental steps, respectively.

As part of the license agreement, the Company issued 17,650 common shares or 15% of the total issued and outstanding shares of PBS, to Dr. Paul Coussens at par value on October 2, 2006. After issuance of the shares, the Company holds 85% of the total issued and outstanding shares of PBS. The Company recorded the fair value of the shares of PBS issued to Dr. Paul Coussens at a nominal value. As PBS had no assets or liabilities, no value was allocated to the minority interest.

The termination date of the sponsored research agreement was July 14, 2007.

On February 2, 2008, the Company, through its subsidiary, Phoenix BioSystems, Inc., entered into an amendment of the above mentioned exclusive worldwide license agreement with Michigan State University for the development of new cell-culture based flu vaccines to protect against the spread of influenza viruses among humans, including potentially the high pathogenicity H5N1 virus.

As of September 30, 2008, total payment of $73,352 has been paid in relation to the project, including the reimbursement of research expenses of $68,353 to MSU.

On November 2, 2007, HepaLife Technologies, Inc. entered into an exclusive license agreement with the U.S. Department of Agriculture, Agricultural Research Service for the use of patented liver cell lines in bioartificial liver devices and in-vitro toxicological testing platforms.

NOTE 7 – EQUIPMENT

	September 30,		December 31,
	2008		2007

Computer equipment	$	-	$	37,382
Furniture and fixtures		-		1,089
		-		38,471
Less: accumulated depreciation		-		(27,589	)
	$	-	$	10,882

During the three months ended September 30, 2008, the Company removed the cost and related accumulated depreciation from the Company’s financial statements for equipment that was either no longer in service or deemed obsolete. Substantially all of this equipment was located at the Company’s administrative office in Vancouver, British Columbia, Canada, which, effective September 1, 2008, was closed. The Company recorded a loss on disposal of fixed assets of $3,060 in the consolidated statements of operations for the three and nine months ended September 30, 2008.

Depreciation expenses charged to operations for the three months and nine months ended September 30, 2008 were $2,607 (2007: $4,177) and $7,820 (2007: $12,078) respectively.

NOTE 8 - SHARE CAPITAL

Under the New Purchase Agreement with Fusion Capital Fund II (“Fusion Capital”) dated January 20, 2006, Fusion Capital had agreed to purchase from the Company up to $15,000,000 of the Company’s share of common stock over a thirty month period. On May 11, 2007, the Company and Fusion Capital mutually terminated the Common Stock Purchase Agreement. The Company did not incur any termination costs as a result of mutually terminating this agreement.

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During the year ended December 31, 2007, Fusion Capital has purchased 891,019 shares of common stock of the Company for total proceeds of $495,001.

On May 23, 2008, the Company completed a private placement (the “Private Placement”) of 10,660,705 units (the "Units") at a price of $0.425 per Unit or approximately, $4,530,800 in the aggregate. Each Unit consisted of one share (collectively, the “Unit Shares”) of the Company’s common stock and one Series C Stock Purchase Warrant to purchase a share of common stock at $0.55 per share for a period of two years from the date of issuance (the “Series C Warrants”). In connection with the Private Placement the Company agreed to file a registration statement for the purpose of registering the Unit Shares and the shares issuable upon the exercise of the Series C Warrants, for resale by the Investors.

The Units were offered and sold to 12 accredited investors (the “Investors”) as defined in Regulation D as promulgated under the Securities Act of 1933, as amended.

Pursuant to the Subscription Agreement and the Registration Rights Agreement, the Company and the investor parties have made other covenants and representations and warranties regarding matters that are customarily included in financings of this nature. In the event that during the twelve month period following the Closing Date, the Company issues shares at a price per share which is less than $0.425 per share (the “Base Share Price”) then the Company is required to issue to the investors the number of shares equal to (1) the quotient of the aggregate purchase price payable under the Securities Purchase Agreement divided by Base Share Price less (2) the quotient of the aggregate purchase price divided by the per share purchase price under the Securities Purchase Agreement.

In connection with the private placement, the agent was due a sales commission equal to $90,828 or two (2%) percent of the gross proceeds, which commission it elected to receive in the form of 213,713 Units. In addition, the Company issued an aggregate of 50,000 Units, in payment of legal fees in the amount of $21,250. These Units were otherwise issued on the same terms and conditions as the Units sold in the Private Placement.

On August 18, 2008, the Board of Directors agreed to issue 400,000 shares of its restricted common stock for services provided by its investment banker for the period January 1, 2008 to August 31, 2008. The value of the issuance was agreed to be the value of services provided, $170,000.

See also Note 4.

NOTE 9 - CONVERTIBLE PROMISSORY NOTE

(i) The Agreement

On May 11, 2007, the Company entered into a Securities Purchase Agreement (the “Agreement”) with GCA Strategic Investment Limited (the “Purchaser”). The Agreement provided for the sale of $2,500,000 aggregate principal amount of the Convertible Note due May 11, 2009 (the “Convertible Note”). The Convertible Note was issued on May 11, 2007 and the purchase price of the Convertible Note was $2,125,000 (eighty-five per cent of the principal amount of the Convertible Note).

In connection therewith, the Company also issued to the Purchaser warrants to purchase up to an aggregate of 670,000 shares of the Company’s common stock at a price of $1.50 per share (the “Warrants”). The Warrants have a term of five years.

The Company also issued 67,000 warrants for payment of related legal fees.

The Convertible Note (and any accrued and unpaid interest or liquidated damages amount) may be converted into shares of the Company's common stock at a conversion price will be 95% of the trading volume weighted average price, as reported by Bloomberg LP (the “VWAP”), for the five trading days immediately prior to the date of notice of conversion.

In 2007, $1,745,000 of Convertible Notes were converted into 2,604,721 shares. During the nine months ended September 30, 2008, the remaining Convertible Notes in the amount of $755,000 were converted into 2,342,415 shares.

During the nine months ended September 30, 2008, $468,343 (2007: $1,092,320) of the discount on issuance of Convertible Note was recorded in the Statement of Operations. At September 30, 2008, all discounts on issuance of Note were amortized.

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NOTE 10 - WARRANTS

As of September 30, 2008, there were 737,000 warrants outstanding (Note 9) and 12,989,830 Series C Warrants outstanding (Note 4 and 8). Each warrant entitles the holder to purchase one share of the common stock of the Company at an exercise price of $1.50 per share until May 11, 2012 and each Series C Warrant entitles the holder to purchase one share of the common stock of the Company at an exercise price of $0.55 per share until May 23, 2010.

On September 30, 2008 the Company decreased the exercise price of the Series C Warrants from $0.55 to $0.35 per share.

The fair value of the 737,000 warrants issued on May 11, 2007 was $714,890 and was estimated using the Black-Scholes option pricing model with assumptions as follows:

Risk free interest rate	4.58%
Expected term	5.0 years
Expected volatility	96.2%
Dividend per share	$0.00

The fair value of the 12,989,830 Series C Warrants issued on May 23, 2008 was $1,898,867 and was estimated using the Black-Scholes option pricing model with assumptions as follows:

Risk free interest rate	2.46%
Expected term	2.0 years
Expected volatility	94.1%
Dividend per share	$0.00

NOTE 11 - STOCK OPTIONS

The Company has an active stock option plan that provides shares available for options granted to employees, directors and others. Options granted to employees under the Company’s option plans generally vest over two to five years or as otherwise determined by the plan administrator. Options to purchase shares expire no later than ten years after the date of grant.

The movement of stock options can be summarized as follows:

						Remaining		Aggregate
				Weighted average		contractual		intrinsic
	Number of options			exercise price		term		value

Outstanding at December 31, 2006		10,350,000		$	0.67
Granted		2,026,750			0.52
Cancelled		(10,350,000	)		0.67
Outstanding at December 31, 2007		2,026,750			0.52
Granted		775,000			0.54
Outstanding at September 30, 2008		2,801,750			0.54		8.71	$	-

Exercisable at September 30, 2008		-		$	0.54

Available for grant at September 30, 2008		34,996,250

The aggregate intrinsic value in the table above represents the total pretax intrinsic value for all “in-the-money” options (i.e. the difference between the Company’s closing stock price on the last trading day of the period ended September 30, 2008 and the exercise price, multiplied by the number of shares) that would have been received by the option holders had all option holders exercised their options on September 30, 2008. Weighted average fair value of options granted during the nine months ended September 30, 2008 was $0.37 (2007: $0.43) per share.

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A summary of the Company’s unvested stock options and changes during the periods is as follows:

	Number of options			Fair value per share

Unvested, December 31, 2006		4,650,000		$	0.51
Granted during 2007		2,026,750			0.43
Cancelled during 2007		(4,650,000	)		0.51
Unvested, December 31, 2007		2,026,750			0.43
Granted during 2008		775,000			0.37
Unvested, September 30, 2008		2,801,750			0.41

On February 1, 2008, the Company granted options to an employee to purchase up to 75,000 shares of the Company’s common stock at an exercise price of $0.37 each. Of the total options, 25,000 options vest upon achieving the first goal of the Company. The remaining options are vested in another 25,000 options each upon achieving each of the three goals set by the Company. The three goals are expected to be achieved on or before July 31, 2009, January 31, 2010 and January 31, 2011 respectively.

The fair value of the 75,000 options granted was estimated at $0.27 each, for a total of amount of $20,250, by using the Black-Scholes Option Pricing Model with the following weighted average assumptions: dividend yield of 0%, expected volatility of 90.53%, risk-free interest rates of 2.75%, and expected lives of 5 years.

On June 11, 2008, the Company granted options to two directors to purchase up to 550,000 shares of the Company’s common stock at an exercise price of $0.61 each. Every 100,000 of the first 500,000 options vest annually starting from October 1, 2008 and every 10,000 of the remaining 50,000 options vest annually starting from June 11, 2009.

The fair value of the 550,000 options granted was estimated at $0.41 each, for a total of amount of $225,500, by using the Black-Scholes Option Pricing Model with the following weighted average assumptions: dividend yield of 0%, expected volatility of 83.39%, risk-free interest rates of 3.49%, and expected lives of 5 years.

On June 18, 2008, the Company granted options to a director to purchase up to 50,000 shares of the Company’s common stock at an exercise price of $0.57 each. Every 10,000 of the 50,000 options vest annually starting from June 18, 2009.

The fair value of the 50,000 options granted was estimated at $0.39 each, for a total of amount of $19,500, by using the Black-Scholes Option Pricing Model with the following weighted average assumptions: dividend yield of 0%, expected volatility of 83.32%, risk-free interest rates of 3.57%, and expected lives of 5 years.

On September 12, 2008, the Company granted options to two directors to purchase up to 100,000 shares of the Company’s common stock at an exercise price of $0.26 each. Every 20,000 of the 100,000 options vest annually starting from September 12, 2009.

The fair value of the 100,000 options granted was estimated at $0.17 each, for a total of amount of $17,000, by using the Black-Scholes Option Pricing Model with the following weighted average assumptions: dividend yield of 0%, expected volatility of 84.15%, risk-free interest rates of 2.97%, and expected lives of 5 years.

During the nine months ended September 30, 2008, compensation expense of $519,578 (2007: $787,648) was recognized for options previously granted and vesting over time and is recorded in Salaries and Benefits on the Consolidated Statements of Operations. As of September 30, 2008, the Company had $342,852 of total unrecognized compensation cost related to unvested stock options.

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The options outstanding and exercisable as of September 30, 2008 can be summarized as follows:

[Missing Graphic Reference]

The Company does not repurchase shares to fulfill the requirements of options that are exercised. Further, the Company issues new shares when options are exercised.

NOTE 12 –SUBSEQUENT EVENTS

On October 3, 2008, the Company acquired assets from Arbios Systems, Inc, in order to enhance and strengthen its PICM-19 porcine liver cell line based bioartificial liver technology. Acquired assets include: patents and licenses; scientific equipment; FDA Investigative New Drug (IND) application; Phase I and Phase II/III clinical protocols and clinical data; and standard operating procedures for manufacturing and quality control. The purchase price consisted of (i) $450,000 in cash, $250,000 was paid at closing and $200,000 has been deferred for up to 18 months, (ii) a Series D warrant to purchase up to 750,000 shares of the Company’s common stock at an exercise price of $0.35 per share for a period of 5 years, and (iii) assumption by the Company of liabilities.

On October 1, 2008, the Company notified the USDA, ARS that the Company has elected to terminate the Cooperative Research and Development Agreement (the “CRADA”) between the Company and the USDA, ARS effective November 30, 2008.

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ITEM 2. Management's Discussion and Analysis of Financial Condition and Results of Operations

Forward-Looking Statements

Except for the historical information presented in this document, the matters discussed in this Form 10-Q for the three and nine months ending September 30, 2008, this report contains forward-looking statements. Such forward-looking statements include statements regarding, among other things, (a) our projected sales and profitability, (b) our growth strategies, (c) anticipated trends in our industry, (d) our future financing plans, and (e) our anticipated needs for working capital. Forward-looking statements, which involve assumptions and describe our future plans, strategies, and expectations, are generally identifiable by use of the words “may,” “will,” “should,” “expect,” “anticipate,” “estimate,” “believe,” “intend,” or “project” or the negative of these words or other variations on these words or comparable terminology. This information may involve known and unknown risks, uncertainties, and other factors that may cause our actual results, performance, or achievements to be materially different from the future results, performance, or achievements expressed or implied by any forward-looking statements. These statements may be found under “Management's Discussion and Analysis of Financial Condition and Results of Operations,” “Business,” “Properties,” as well as in this report generally. Actual events or results may differ materially from those discussed in forward-looking statements as a result of various factors, including, without limitation, the risks outlined under “Risk Factors” and matters described in this report generally. In light of these risks and uncertainties, there can be no assurance that the forward-looking statements contained in this filing will in fact occur.

Overview

We are a development stage biotechnology company focused on the identification and development of cell-based technologies and products. We currently do not directly conduct any of our research and development activities. Rather, once a technology has been identified, we fund the research and development activities relating to the technology with the intention of ultimately, if warranted, licensing, commercializing and marketing the subject technology. Currently, we are concentrating our sponsored research and development efforts on developing a cell-supported artificial liver device, in-vitro toxicology and pre-clinical drug testing platforms.

Artificial Liver Device

We are working towards optimizing the hepatic (liver) functionality of a porcine cell line, and subclones thereof, which we refer to as the “PICM-19 Cell Line.” The PICM-19 Cell Line was developed and patented by USDA Agricultural Research Service scientists. On November 2, 2007, we entered into an exclusive license agreement with the U.S. Department of Agriculture, Agricultural Research Service for the use of this patented technology. The hepatic characteristics of the PICM-19 Cell Line have been demonstrated to have potential application in the production of an artificial liver device, which application was also developed and patented by USDA Agricultural Research Service scientists for potential use by human patients with liver failure.

On October 3, 2008, in order to enhance and strengthen our PICM-19 porcine liver cell line based bioartificial liver technology, we acquired assets from Arbios Systems, Inc., which includes: over 12 patents and patent licenses; miscellaneous scientific equipment; FDA Investigative New Drug (IND) application, including orphan drug and fast track designation; Phase I and Phase II/III clinical protocols and clinical data; and standard operating procedures for manufacturing and quality control. The acquired assets relate to a bioartificial liver device formerly known as “HepatAssist.” HepatAssist was evaluated in the largest-ever Phase II/III clinical study (prospective randomized trial involving over 170 patients) to test the safety and efficacy of a bioartificial liver assist device. The clinical data was published in 2004.

In-Vitro Toxicology Testing

The PICM-19 Cell Line, grown in-vitro, can synthesize liver specific proteins such as albumin and transferrin, and display enhanced liver-specific functions, such as ureagenesis (conversion of ammonia to urea) and cytochrome P450 (a family of over 60 enzymes the body uses to break down toxins and make blood) activity. The P-450 enzyme systems are key components in the overall hepatic detoxification pathway of drugs and other xenobiotics (toxic foreign chemicals which can be both man-made and natural chemicals, such as pesticides and pollutants). Likewise, ureagenesis is another important hepatic function since urea production is required for the detoxification of ammonia derived from the catabolism (breakdown of complex organic molecules into simpler components) of a number of nitrogen-containing compounds. As a result, we believe the PICM-19 Cell Line could be an important element in developing in-vitro toxicological and pre-clinical drug testing platforms that could more accurately determine the potential toxicity and metabolism of new pharmacological compounds in the liver.

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Cell Based Vaccine Production

We are working towards commercializing a chicken cell line, and subclones thereof, which we refer to as the “PBS-1 Cell Line.” The PBS-1 Cell Line was developed for use in cell-based vaccine production and was exclusively licensed from Michigan State University in June 2006. Successful cell-culture based vaccine production has the potential to reduce manufacturing time compared to traditional influenza vaccine manufacturing methods and could allow for rapid expansion of vaccine production in the face of an influenza pandemic.

Currently, traditional vaccine production involves injecting a small amount of a targeted virus into fertilized chicken eggs. Over time, the virus is harvested from the eggs, eventually inactivated and purified, and finally blended into a vaccine and bottled in vials. This egg-based production method takes at least six months, and in the event of a flu pandemic, it is unlikely to produce vaccines fast enough to meet expected demand.

Third-party analysis has confirmed that PBS-1 cells are free from exogenous (from outside the system) agents, fungi, bacteria, diseases, and potentially harmful viruses. In addition, PBS-1 cells have grown and replicated several human influenza virus types, including H1N1, H3N2 and type B. The most important step towards the production of a cell-culture based vaccine against a targeted virus is the ability to efficiently grow the same virus in a cell substrate.

Critical Accounting Policies

Our discussion and analysis of our financial condition and results of operations are based on our financial statements, which have been prepared in accordance with accounting principles generally accepted in the United States. The preparation of these financial statements requires us to make estimates and judgments that affect the reported amounts of assets, liabilities and expenses and related disclosures. We review our estimates on an ongoing basis.

We consider an accounting estimate to be critical if it requires assumptions to be made that were uncertain at the time the estimate was made; and changes in the estimate or different estimates that could have been made could have a material impact on our results of operations or financial condition.

General and Administrative Expenses

Our general and administrative expenses consist primarily of personnel related costs, legal costs, including intellectual property, investor relations costs, stock based compensation costs, accounting costs, and other professional and administrative costs.

Research and Development Costs

Research and development costs represent costs incurred to develop our technology incurred pursuant to our CRADA with the USDA’s Agricultural Research Service and pursuant to our sponsored research agreement with MSU. The agreements include salaries and benefits for research and development personnel, allocated overhead and facility occupancy costs, contract services and other costs. We charge all research and development expenses to operations as they are incurred, except for prepayments, which are capitalized and amortized over the applicable period. We do not track research and development expenses by project. In addition costs for third party laboratory work might occur.

		Hepalife Technologies, Inc.
		(Registrant)


Date	Signature	Title

November 14, 2008	/s/ Frank Menzler	Director, President, CEO, CFO
	Frank Menzler