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Final Results

26 Jun 2007 07:00

Embargoed: 0700hrs, 26 June 2007

Akers Biosciences, Inc. ("Akers" or the "Company") Preliminary Results for the Year Ended 31 December 2006

Chairman's and CEO's Statement

Results

Since reporting that the Company expected 2006 revenues to be $5.2 million, the Company has acquired the assets of its major distributor of breathalyzers to the US Military, `Bout Time Marketing ("BTM"). As a consequence of the accounting treatment of this acquisition, which is explained below, the Company's 2006 revenues were in fact $1.0 million (2005: $4.6 million).

Under the terms of the acquisition, Akers acquired the assets of BTM which, amongst other things, included an inventory of products supplied by Akers but not yet shipped to BTM's customers. As part of the audit process, the Company's auditors reviewed the accounting treatment associated with this acquisition and requested that the Company commission an independent valuation report on the intangible assets of BTM, in part to ascertain the revenues that could be recognized by the Company in the 2006 financial year. The independent valuation report was finalized at the end of last week and substantiated the price paid by the Company, both for BTM and WNCK, Inc. The Company's auditors have subsequently reviewed the valuation report and informed the Board that only the sale proceeds of breathalyzers that were actually shipped by BTM to the end user (the US Military) in the 2006 financial year could be recognized in the Company's 2006 accounts.

2006 revenues primarily comprise:

* initial sales of the Company's Heparin/Platelet Factor-4 antibodies test into a small hospital customer base which, with very satisfactory product acceptance by clinicians, is expected to contribute significantly to future growth; * alcohol breathalyzer sales, but most importantly initial sales of approximately $500,000 to the US Military.

While the revenues reported here are extremely disappointing, the Board expects to realize the balance of the full $4.2 million in the 2007 financial year. The Company has already realized $1.5 million of this revenue during H1 2007, from sales of breathalyzers to the US Military, and expects to receive further contracts.

The Company's pre-tax loss was $9.6 million (2005: pre-tax loss of $4.5 million). This figure was adversely affected by the Company recording a significant bad debt from a distributor, the financial impact of which, although painful, is expected to be ameliorated by the Company taking back into inventory the product, with the intention of re-sale.

Business Review

All of the Company's proprietary technologies provide the platform for high margin niche products, intended for use in specialized market segments. These market segments include: clinical laboratories, homeland security, military, OTC, industrial and consumer safety, doctor's surgeries, and clinical research.

Revenues in 2007 will be primarily due to the market penetration of four of the Company's products, which are detailed here.

PIFA‚® Heparin Platelet Factor 4 Rapid Assay

The Company's rapid HPF4 test is sold into the US clinical laboratory market through Cardinal Health and Corgenix Medical Group under the Company's brand "PIFA‚® Heparin/PF-4 Rapid Assay". This is the first rapid test for HPF4 antibodies, and the product is protected by two of the Company's patents, with additional patents pending. The market response clearly indicates a significant clinical need for the product, and several studies have been presented at scientific meetings indicating that the Company's test may be more accurate than any competitor on the market.

Cardinal Health has signed a new contract with the Company for the distribution of this product. This evergreen agreement guarantees that the product will remain in Cardinal's highest focus of products at least through 2008, and that the Company will be in the highest tier of supplier relationships. In addition, the agreement provides a price increase beginning 1 August 2007 and for the distribution of additional products.

As background, heparin is the most widely used intravenous anticoagulant, and is commonly used for the prophylaxis and treatment of thromboembolic disease, as well as numerous other applications including certain types of lung and heart disorders, and during or after a variety of surgeries including open heart, bypass, dialysis and orthopedic procedures. Patients with recent exposure to heparin are at a much greater risk for developing Heparin-Induced Thrombocytopenia ("HIT"), than are those not having previously been given the drug. The Company's test detects the presence of Heparin/PF-4 antibody, which is associated with patients at risk for HIT, and is rapidly becoming a standard of care in hematology and cardiology.

The Company and its partners have initially promoted the use of the test as a replacement for current laboratory tests used in the detection of a heparin "allergy" or other serious thrombolytic reaction resulting from heparin treatment. The Company's product has significant advantages both in terms of cost and time to result. The Company's test takes minutes to perform, while the current laboratory tests take hours to perform on complex instrumentation. HIT can rapidly progress in minutes or hours, and can result in death or dismemberment. The Company's product is the only test available on the market that can provide real-time in formation that can be useful in formulating a clinical diagnosis. In 2006, over 3.5 million tests were performed using current laboratory tests to confirm a potential "heparin allergy" or HIT, primarily in cardiology and emergency medicine patients.

The Company has expanded its customer base through new distribution relationships in the UK and Europe. In addition, the Company plans to distribute the product to the US physicians' office market through new distributors in 2007.

Breath Alcohol‚® and BreathScan‚® Alcohol Breathalyzers

The Company is the only manufacturer of portable, disposable alcohol breathalyzers in the US. The Company is continuing to pursue sales of its Alcohol Breathalyzers through its own Breath Alcohol ‚® brand and the recently acquired BreathScan‚®. These sales are generated through a rapidly expanding distributor network, as well as through direct sales.

In February, 2006, the Company acquired certain assets of WNCK, Inc., ("WNCK") of The Woodlands, Texas, USA, in an effort to strengthen its position in the alcohol breathalyzer industry. WNCK had been the leading distributor of disposable alcohol breathalyzers in the U.S., and the Company had been the sole manufacturer of WNCK's products for the past 5 years.

Through this acquisition, the Company now owns the BreathScan product line, one of the industry standards for the past 15 years, and WNCK's customer base. The Company has already benefited from increased margins as well as direct distribution channels, which are likely to have a synergistic effect with other products.

This is especially important in view of rapidly expanding markets resulting from new Coast Guard regulations and US Military safety programs. One of the Company's marketing partners, `Bout Time Marketing ("BTM") has helped develop a special safety program for the US Military, and is a significant distributor of disposable alcohol breathalyzers to the U.S. Military and retail markets. Its Legal Limit product line and Alcohol Safety Program were amongst the first products to address responsible alcohol consumption by solders and civilians.

In January, 2007 the Company acquired certain assets of BTM, and now owns the Legal Limit product line, and BTM's customer base. The Company has already benefited from increased margins and distribution channels, and has received contracts with the US Military in 2006 and 2007. The Board expects that additional contracts will be received in 2007, and that a stable, recurring business will be achieved in future years. On 19 June, 2007, the US Patent and Trademark Office issued a Notification of Allowance for a patent for certain features of the Legal Limit product, further strengthening this product line.

In addition to being profit-enhancing from the day of closing, these acquisitions have established the Company as the premier force in portable alcohol breathalyzers in the U.S.

Moreover, these acquisitions represent initial steps in the Company's strategy to transform the portable alcohol breathalyzer industry. The Company has positioned its breathalyzers as security and safety devices by enhancing the technology through the development of electronic readers. The Company believes that this new product positioning, together with the addition of the Legal Limit products will enhance market penetration and profit margins.

Additional applications of the breathalyzer product line include a program to curb driving under the influence of alcohol used by the Italian government. The Company's distributor in the UK, Advanced Rapid Diagnostics, Ltd., has also had success in selling the product into the industrial safety sector. Also, the DOT approval announced in September, 2006 opened the maritime safety industry to the Company's breathalyzer products.

TriCholesterol‚®

The Tri-Cholesterol Test Kit is the only FDA-approved rapid assay that provides a complete cholesterol profile of the patient, with semi-quantitative determinations of high-density lipoprotein (HDL) cholesterol, low-density lipoprotein (LDL) cholesterol, and total cholesterol levels in whole blood obtained from a finger stick. The Company is currently marketing this product through new distribution channels due to the unsatisfactory performance of its former distributor. The Company plans to re-launch this product with a new distributor in the second half of 2007, and believes that there is still significant market potential.

In addition, the Company has further developed this product into a format suitable for doctor's offices, TriCholesterol ‚®Pro. The Company is in discussions with several US physicians' office distributors, and plans to introduce the product to this new market in the second half of 2007.

Battlefield Blood Transfusion Card

The ABO Blood Group was the first to be identified and is the most significant for transfusion practice. Accurate testing of donor and recipient blood for ABO /D compatibility is essential for the prevention of hemolytic transfusion reactions. To respond to the unpredictable demands of battlefield transfusion support, the U.S. Military may use "the walking blood bank" as its blood supply. This requires on site identification of the donor and recipient blood types. The Battlefield Blood Transfusion Card can accomplish this task using only the card, a drop of blood, and a drop of a rinse reagent.

Following several successful clinical trials, the Company has received several small orders from the US Military for this product. The demand for the product is expected to grow significantly since over 40% of blood transfusions in the military theatre of operations are performed under field conditions, and there is currently no other rapid test competition. The Company is in discussions with the US Military to expand the use of the product under field conditions.

Financials:

Share Issues

During January and again in November and December 2006, three of the Company's independent directors received an aggregate of 147,459 shares of the Company's common stock as payment for directors fees and other fees owing to them at the time of issuance in the amount of $145,012.

On 27 February 2006, WNCK, Inc. received 125,000 shares of the Company's common stock as partial consideration for the Company's purchase from WNCK of its trademark and customer and distributor lists.

During the second half of 2006, Brittany Capital converted the $2,770,000 of Convertible Notes outstanding at 31 December 2005 plus Original Issue Discount plus Premium plus accrued interest thereon into 4,279,168 shares of the Company's common stock.

Other Income

The Company was able to continue to take advantage of a program in the State of New Jersey wherein companies that incur net operating losses are able to sell their state NOL's at a nominal discount to their implied value. The benefit recognized for 2006 was $0.5 million vs. $0.3 for 2005.

Liquidity and Cash Resources

As of 31 December 2006, the Company had yet to generate positive cash flow from its own operations due to the preliminary nature of such operations, substantial ongoing investment in research and development efforts, and expenditures to build the appropriate infrastructure to support its expected growth. Consequently, the Company has been substantially dependent on the issuance of convertible debt securities and borrowing from its revolving credit facility with the Company's cash.

The Company issued $2.0 million of new Convertible Notes to Brittany during 2006 and drew down $0.95 million against its revolving credit facility to partially fund its 2006 loss.

During May 2007, the Company refinanced the Convertible Notes due to Brittany at 31 December 2006, as well as approximately $1.3 million borrowed during the first five months of 2007 from Brittany. Brittany issued new Convertible Notes which extend the maturity of the 2006 and 2007 Notes until 31 December 2008 and which permit the Company to draw up to an additional $1,000,000 during the second half of 2007. This facility, supplemented by expected NOL sales at equal to or higher levels than during 2006 and a continuation of the higher level of revenue experienced during the first half of 2007, should provide the liquidity the Company needs to meet its obligations during the next 12 months.

Personnel

As part of its objective of strengthening its management team the Company has made significant management changes with the appointment of very experienced executives. Thomas A. Nicolette has joined the company as President, and is responsible for the operations of the business and Arthur Mullin has replaced Paul Freedman as Chief Financial Officer. It is appropriate for the Board of Directors to recognise the contribution Paul Freedman has made to the Company over many years and to thank him for his all his efforts and dedication.

Product Development

The Company now offers six different proprietary platform technologies, and has developed products based on these technologies.

During 2006, the Company proceeded with the development of products for its new Homeland Security suite of rapid tests. These include the environmental detection of anthrax (Bacillus anthracis) and plague (Yersinnia pestis), and a High Pathogencity BioScreen Assay, which could be used for mass screening in the event of an outbreak of avian flu or biowarfare agents. All of these products are based on the Particle ImmunoFiltration Assay technology, and are packaged in a format similar to its PIFA Heparin/PF-4 test.

In addition, the Company completed the development of the Battlefield Blood Transfusion Card, and introduced this product to the US Military. The Company is also currently in discussion with the military regarding the development of a multi-screen theatre card.

Current Trading and Outlook

The Company has achieved significant milestones in the market penetration of two of its key products in 2006, and plans to re-launch its cholesterol test in 2007. The Company has restructured its debt in 2007, and is financially stable. The acquisitions completed in 2006 and early 2007 have shown the significant potential of the alcohol breathalyzer business, and the Company has already received two military contracts. These acquisitions have made the Company a premier force within the industry, and have put the Company on a positive future revenue track. If US Military contracts are obtained as expected in 2007, the Company will produce its first operating profit in its history.

David WilbrahamChairmanRaymond F. Akers, Jr., Ph.D.President and CEOAkers Biosciences, Inc.Financial Statements

Consolidated Balance Sheets as at 31 December 2006 and 2005

2006 2005 Assets Current Assets Cash $ 41,142 $ 3,173,017 Trade receivables, net of allowance for doubtful accounts of $452,916 and $963,630 in 2005 and 2004, 617,036 3,203,777respectively Inventories 1,106,941 1,219,275 Prepaid and other current assets 228,458 147,333 Total current assets 1,993,577 7,743,402 Property and Equipment, net 224,464 246,580 Other Assets Patent costs, net of accumulated amortization 82,803 97,119 Other intangibles 657,641 - Deferred financing costs, net of accumulated 31,847 135,456amortization Deposits and other assets 12,632 12,632 Total other assets 784,923 245,207 $ 3,002,964 $ 8,235,189 Liabilities and Stockholders' Deficiency Current Liabilities Accounts payable and accrued expenses $ 1,817,062 $ 1,611,122 Accrued interest payable 174,006 117,547 Notes payable 3,251,098 2,903,478 Current portion of long-term debt 29,964 38,731

Current portion of obligations under capital leases 12,829 12,829

Total current liabilities 5,284,959 4,683,707 Long-Term Debt Long-term debt, net of current portion 384,699 414,663 Obligations under capital leases, net of current 1,845 13,080portion Total long-term debt 386,544 427,743 Stockholders' Equity(Deficiency) Preferred stock, no par value Authorized 15,000,000 shares, no shares issued and outstanding at December 31, 2006 and 2005 - - Common stock, no par value Authorized 80,000,000 shares issued and outstanding 59,806,044 and 55,762,885 shares at December 31, 2005 and 2004 62,593,546 58,790,850 Accumulated deficiency (65,262,085) (55,667,111) Total stockholders' equity (deficiency) (2,668,539) 3,123,739 Total Liabilities and Stockholders' Equity $ 3,002,964 $ 8,235,189(Deficiency)

Consolidated Statements of Operations for years ended 31 December 2006 and 2005

2006 2005 Revenues $ 1,019,629 $ 4,610,567 Cost of production 2,463,999 2,939,836 Gross profit(loss) (1,444,370) 1,670,731

Sales and general and administrative 6,485,299 3,087,316 expenses

Research and development expenses 786,676 789,750 Total expenses 7,271,975 3,877,066 Loss from operations (8,716,345) (2,206,335) Other income (expense) Interest income 19,062 10,529 Litigation recovery - 713,046 Forgiveness of trade payables - 9,472 Sale of New Jersey NOL's 483,086 304,533 Loss on disposal of property and - (328)equipment

Foreign currency transactions income (13,078) 1,240 (loss)

Interest expense (1,256,227) (650,009) Total other income (expense) (767,157) 388,483

Net loss before US GAAP adjustment (9,483,502) (1,817,852)

US GAAP adjustment for equity (111,472) (2,688,759)compensation for options and warrants issued Net loss $(9,594,974)$(4,506,611)

Consolidated Statements of Stockholders' Equity (Deficit)

Preferred Common Stock Accumulated Stock Shares Amount Shares Amount Deficiency Total Balance, December 31, - - 46,955,614 $ $ $2004 48,366,016 (51,160,500) (2,794,484) Issuance of stock for - - 2,627,306 2,291,750 - 2,291,750cash Issuance of warrants - - - 2,688,759 - 2,688,759for products and services Issuance of common - - 5,931,746 5,207,000 - 5,207,000stock in exchange of debt Issuance of common stock in exchange of trade payables - - 248,219 237,325 - 237,325 Net loss for the year - - - - (4,506,611) (4,506,611)ended December 31, 2005 Balance, December 31, - $ - 55,762,885 $ $ $ 3,123,7392005 58,790,850 (55,667,111) Issuance of stock for - - 125,000 148,365 - 148,365acquisition Issuance of warrants - - 147,459 256,484 - 256,484for products and services Issuance of common - - 4,312,234 3,397,847 - 3,397,847stock in exchange of debt Net loss for the year - - - - (9,594,974) (9,594,974)ended December 31, 2006 Balance, December 31, - $ - 60,347,578 62,593,546 (65,262,085) (2,668,539) 2006

Statements of Cash Flows for the years ended 31 December 2006 and 2005

2006 2005 Cash Flows From Operating Activities Net loss $ (9,594,974) $ (4,506,611) Adjustments to reconcile net loss to cash used in operating activities: Depreciation and amortization 199,095 101,139 Amortization of deferred finance costs 140,456 209,369 Stock, stock options and warrants issued to 111,472 2,688,759employees and non-employees Adjustments for litigation recovery - (713,046) Provisions for bad debts 2,804,149 182,267 Changes in operating assets and liabilities: (Increase) decrease in: Trade receivables (217,408) (3,280,062) Inventories 112,334 (599,629) Prepaids and other current assets (81,125) 69,776 Increase (decrease) in: Accounts payable and accrued expenses 990,508 234,416 Net cash used in operating activities (5,305,493) (5,613,622) Cash Flows From Investing Activities Purchase of property and equipment (64,629) (87,968) Purchase of intangible assets (607,310) - Net cash used in investing activities (671,939) (87,968) Cash Flows From Financing Activities Proceeds from issuance of stock, net - 10,000 Proceeds from warrants exercised - 2,543,750 Proceeds from borrowings 4,532,145 10,039,043 Repayments of capital lease obligations (11,235) (7,788) Repayments on borrowings (1,638,506) (3,552,852) Deferred financing costs (36,847) (340,000) Net cash provided by financing activities 2,845,557 8,692,153 Increase (decrease) in cash (3,131,875) 2,990,563 Cash, beginning of year 3,173,017 182,454 Cash, end of year $ 41,142 $ 3,173,017

Consolidated Statements of Cash Flows for the years ended 31 December 2006 and 2005 (continued)

2006 2005 Supplemental Disclosures of Cash Flow Information: Non-cash investing and financing activities are as follows:

Conversion of debt and accrued interest payable $ 3,397,847 $ 5,108,989 to common stock

Conversion of trade payable to common stock $ 145,012 $ 73,336 Issuance of stock for acquistion $ 148,365 $ - Equipment purchased under capital lease $ - $ 17,569 Cash Paid During the Period for Interest $ 175,280 $ 66,933

Summary of Significant Accounting Policies

The Summary of Significant Accounting Policies below are integral parts of the accompanying Consolidated Financial Statements.

Description of Business: Akers Biosciences, Inc. and its subsidiaries (the "Company" or "Akers") is a New Jersey Corporation, which was incorporated on March 8, 1989. The Company commenced research and development operations in September 1989, and until 2003 had devoted substantially all its efforts to establish the new business.

Patents and Trade Secrets: The Company has developed several diagnostic tests that can detect the presence of various substances in a person's blood, urine and saliva. Proprietary protection for the Company's products, technology and process is important to its competitive position. To date, the Company has received four patents from the United States Patent Office (5,565,366, 5,231,035, 5,827,749, and D368045). Other patents have been granted through the World Patent Cooperation Treaty ("PCT") (WO 92/05440, US2005/027822, US2005/ 015875, US91/06870, and US2005/036109), European Patent Convention (EP 0 556 202 B1), and in Japan (516757/91). Patents are in the national phase of prosecution in many PCT-participating countries. Additional proprietary technology consists of numerous different inventions. The Company intends to file additional patent applications, where appropriate, relating to new products, technologies and their use in the US, European and Asian markets. Management intends to protect all other intellectual property (e.g., copyrights, trademarks and trade secrets) using all legal remedies available to the Company.

Principles of Consolidation: The consolidated financial statements include the accounts of the Company and its subsidiaries. All significant intercompany balances and transactions are eliminated. The subsidiaries are currently asset holding companies and have no direct operations at this time.

Revenue Recognition: The Company recognizes sales at the time goods are shipped.

Trade Receivables: Trade receivables are carried at original invoice amount less an estimate made for doubtful receivables based on a review of all outstanding amounts. Management determines the allowance for doubtful accounts by regularly evaluating individual customer receivables and considering a customer's financial condition, credit history, and current economic conditions. Trade receivables are written off when deemed uncollectable. Recoveries of trade receivables previously written off are recorded when received. Trade receivables are considered to be past due if any portion of the receivable balance is outstanding for more than 90 days. Management may elect to charge interest on past due trade receivables.

Inventories: Inventories are stated at the lower of cost (first-in, first-out) or market , and primarily consist of finished goods.

Property and Equipment: Property and equipment are stated at cost. Depreciation and amortization are computed over the estimated useful lives of the respective assets using straight-line and accelerated methods. Upon sale or retirement of assets, the related costs and accumulated depreciation are eliminated from the accounts and the resulting gain or loss is included in operations. Expenditures for repairs and maintenance that do not increase the useful lives of the assets are charged to operations as incurred.

Patent Costs: Costs associated with applying for patents are capitalized as patent costs. Once the patents are approved, the respective costs are amortized over a period of twelve to seventeen years on a straight-line basis. Patent pending costs for patents that are not approved are charged to operations the year the patent is rejected. Accumulated amortization related to patents was $148,682 and $134,366 as of December 31, 2006 and 2005, respectively. Amortization expense amounted to $14,316 and $20,811 for the years ended December 31, 2006 and 2005, respectively.

Deferred Financing Costs: Costs incurred in connection with financing have been capitalized and are being amortized on the straight-line basis over the term of the related debt. As of December 31, 2006 and 2005, accumulated amortization was $28,949 and $27,018, respectively. As of December 31, 2006 all deferred finance costs from long term debt has been fully amortized. Amortization expense for each of the years ended December 31, 2006 and 2005 was $1,931 and $2,895, respectively. Short term financing charges are expensed over the life of the loan as additional interest expense and any unexpensed amounts at year end are included as deferred financing costs. The balance of $133,536 was expensed in 2006. As of December 31, 2006 $31,847 of financing costs related to short obligations remain on the books and will be expensed in 2007.

Research and Development Costs: Research and development costs are charged to operations when incurred.

Advertising and Promotion: Advertising and promotion costs are charged to current operations when incurred. Advertising and promotion costs for the years ended December 31, 2006 and 2005 were $85,979 and $11,422, respectively.

Stock-Based Compensation: SFAS No. 123, as amended, "Accounting for Stock-Based Compensation ("SFAS No. 123") requires expanded disclosures of stock-based compensation cost to be measured based on the fair value of the equity instrument awarded. This standard allows the Company, and the Company has elected, to measure compensation cost for these plans through December 31, 2005 using the intrinsic value based method of accounting prescribed by the Accounting Principles Board Opinion No. 25, "Accounting for Stock Issued to Employees ("APB 25"). As of December 31, 2005, all stock options were vested. Beginning in January 1, 2006, the Company has adopted as required the provisions of SFAS No.123(R) for all outstanding options under the prospective method. Under the prospective method, noting the Company previously applied APB 25 using the minimum value method, the Company is not required to recognize compensation expense going-forward for non-vested options as of December 31, 2005. Beginning January 1, 2006, the company is required to recognize compensation costs fro all share-based payments granted equal to the fair value over the vesting period of each award.

Income Taxes: Deferred income taxes are provided on a liability method. Whereby deferred tax assets are recognized for deductible temporary differences and deferred tax liabilities are recognized for taxable temporary differences. Temporary differences are the differences between the reported amounts of assets and liabilities and their tax bases. Deferred tax assets are reduced by a valuation allowance when, in the opinion of management, it is more likely than not that some portion or all of the deferred tax assets will not be realized. Deferred tax assets and liabilities are adjusted for the effects of changes in tax laws and rates on the date of enactment.

Stock Options and Warrants: The Company's intention is to issue stock options and warrants at no less than fair market value on the date of grant. On infrequent occasions, stock options have been issued at less than fair market value for services and in connection with financings, and the effect of these issuances has been recorded as an expense in the period of issuance of the option. Under US GAAP rules, options or warrants issued to non-employees must be valued based on the Black-Sholes model, or another acceptable measurement procedure, with the calculated fair value to be charged to the statement of operations on the date of issuance. Previously, the fair market value of common stock had been determined based on the price that the Company has received for the issuance of stock to investors during a comparable time period. Since May 22, 2002, fair market value is deemed to be the price of the company's shares as quoted on the Alternative Investment Market of the London Stock Exchange.

Use of Estimates: The preparation of financial statements in conformity with accounting principles generally accepted in the United States of America 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. Actual results could differ from those estimates.

Loss per share: Basic loss per share of $0.17 (2005: $0.09) has been calculated by dividing the net loss for the year of $9,594,974 (2005; $4,506,611) by the weighted average number of shares in issue during the period of 56,787,413 (2005: 50,079,576).

Enquiries:

Dr. Ray Akers, Chief Executive Officer

Thomas Nicolette, PresidentTel. 001 856 848 8698Ben SimonsHansard GroupTel. 020 7245 1100Xavier de MolDan WebsterBridgewell LimitedTel. 020 7003 3000

AKERS BIOSCIENCES INC
Date   Source Headline
6th Mar 20197:00 amRNSResult of Special Meeting of Shareholders
6th Feb 20199:00 amRNSHolding in Company
6th Feb 20197:01 amRNSForm DEFA14A Filing - Additional Proxy Materials
6th Feb 20197:00 amRNSNotice of Special Meeting of Shareholders
5th Feb 20191:00 pmRNSFurther Re. Directorate Change
28th Jan 20197:00 amRNSForm PRE 14A Filing
28th Dec 20183:45 pmRNSDirector/PDMR Shareholding
19th Dec 20184:45 pmRNSIntention to Delist from AIM
18th Dec 20186:00 pmRNSIssue of Equity
10th Dec 20187:00 amRNSResult of AGM & Form 8-K Filing
26th Nov 20182:00 pmRNSFurther Re. Notice of AGM
19th Nov 20182:00 pmRNSFurther Re. Strategic Update
16th Nov 20184:00 pmRNSReverse Stock Split Update
15th Nov 20187:00 amRNSNotice of AGM
15th Nov 20187:00 amRNS3rd Quarter 2018 Results
12th Nov 20187:00 amRNSForm 8-K Filing
8th Nov 20187:30 amRNSSuspension - Akers Biosciences, Inc.
8th Nov 20187:00 amRNSTemporary Suspension of Share Trading on LSE
7th Nov 20182:50 pmRNSStrategic Update & Reverse Stock Split
2nd Nov 20184:15 pmRNSIssue of Equity - Completion & Form 8-K/A Filing
2nd Nov 201810:52 amRNSUpdate Re Issue of Equity
31st Oct 20181:35 pmRNSIssue of Equity & Form 8-K
19th Oct 20182:53 pmRNSForm 8-K Filing
19th Oct 20187:00 amRNSDirectorate Change
12th Oct 20187:00 amRNSForm 8-K/A Filing & Other Updates
8th Oct 20187:00 amRNSDirectorate Change & Other Information
13th Sep 20187:00 amRNSDirectorate Change - Form 8-K Filing
15th Aug 20187:00 amRNS2nd Quarter & H1 2018 Results
27th Jul 20183:00 pmRNSHolding(s) in Company
26th Jul 20187:30 amRNSRestoration - Akers Biosciences Inc.
26th Jul 20187:00 amRNSMailing of 2017 Annual Report
20th Jul 20183:05 pmRNSIssue of Equity
20th Jul 20183:00 pmRNSCorrection: Issue of Equity
18th Jul 201812:00 pmRNSIndependent Sales Representative Agreements - PIFA
16th Jul 20187:03 amRNS1st Quarter 2018 Results
16th Jul 20187:02 amRNSFinal Results 2017 (Restated)
16th Jul 20187:01 amRNS3rd Quarter 2017 Results (Restated)
16th Jul 20187:00 amRNS2nd Quarter 2017 Results (Restated)
3rd Jul 201812:00 pmRNSIndependent Sales Representative Agreements - PIFA
2nd Jul 20187:30 amRNSSuspension - Akers Bioscience, Inc
29th Jun 20187:00 amRNSTemporary Suspension
21st Jun 20187:00 amRNSNotification of Class Action
20th Jun 20187:22 amRNSForm 8-K Filing
18th Jun 20187:00 amRNSForm 8-K Filing
6th Jun 20187:00 amRNSForm 8-K/A Filing
4th Jun 20187:00 amRNSForm 8-K Filing
31st May 20187:25 amRNSUpdate Re. Nasdaq Minimum Bid Price Requirement
29th May 20187:00 amRNSDirectorate Change
29th May 20187:00 amRNSWithdrawal of 510(k) Submission - Chlamydia Assay
29th May 20187:00 amRNSNotice of Form 10-Q Filing Delinquency from Nasdaq

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