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&lt;p style='margin-top:0in;margin-right:0in;margin-bottom:6.0pt;margin-left:0in;text-indent:20.0pt;text-align:justify;text-indent:.25in'&gt;The Company generates revenue primarily from (i) the sale of polymer products and (ii) license, royalty and development agreements.&lt;/p&gt; &lt;p style='margin-top:0in;margin-right:0in;margin-bottom:6.0pt;margin-left:0in;text-indent:20.0pt;text-align:justify;text-indent:.5in'&gt;&lt;u&gt;Product Sales&lt;/u&gt;&lt;/p&gt; &lt;p style='margin-top:0in;margin-right:0in;margin-bottom:6.0pt;margin-left:0in;text-indent:20.0pt;margin-left:.25in;text-align:justify;text-indent:.25in'&gt;Revenues generated from the sale of polymer products is recognized upon shipment, provided that a purchase order has been received or a contract has been executed, there are no uncertainties regarding customer acceptance, the sales price is fixed or determinable and collection is deemed reasonably assured.&amp;#160; If uncertainties regarding customer acceptance exist, the Company recognizes revenues when those uncertainties are resolved and title has been transferred to the customer.&amp;#160; Amounts collected or billed prior to satisfying the above revenue recognition criteria are recorded as deferred revenue.&lt;/p&gt; &lt;p style='margin-top:0in;margin-right:0in;margin-bottom:6.0pt;margin-left:0in;text-indent:20.0pt;text-align:justify;text-indent:.5in'&gt;&lt;u&gt;License, Royalty and Development Fees&lt;/u&gt;&lt;/p&gt; &lt;p style='margin-top:0in;margin-right:0in;margin-bottom:6.0pt;margin-left:0in;text-indent:20.0pt;margin-left:.25in;text-align:justify;text-indent:.25in'&gt;The Company also receives license, royalty and development fees, pursuant to agreements with its customers, for the use of its proprietary polymer biomaterials.&amp;#160; The terms of the various license, royalty and development agreements may contain multiple deliverables which may include (i) licenses to use the Company&amp;#146;s polymer biomaterials in the customer&amp;#146;s end-product medical device, (ii) research and development activities, (iii) services and/or (iv) the manufacturing of polymer biomaterials.&amp;#160; Payments to the Company under these agreements may include non-refundable license fees, payments for research and development activities, payments for the manufacture of polymer materials, payments based upon the achievement of certain milestones, payments for the use of the Company&amp;#146;s polymer biomaterials in the customer&amp;#146;s end-product, and/or royalties earned on the sale of the customer&amp;#146;s end-product.&lt;/p&gt; &lt;p style='margin-top:0in;margin-right:0in;margin-bottom:6.0pt;margin-left:0in;text-indent:20.0pt;margin-left:.25in;text-align:justify;text-indent:.25in'&gt;In October 2009, the FASB issued Accounting Standards Update (&amp;#147;ASU&amp;#148;) 2009-13, &lt;i&gt;&lt;font style='font-style:italic'&gt;&amp;#147;Multiple-Deliverable Revenue Arrangements (&amp;#147;ASU 2009-13&amp;#148;).&amp;#148;&lt;/font&gt;&lt;/i&gt;&amp;#160; The Company adopted the provisions of the new multiple-element arrangement guidance summarized in ASU 2009-13 on April 1, 2011 on a prospective basis.&amp;#160; Therefore, this guidance is applicable to any contract entered into or modified on or subsequent to the date of adoption.&amp;#160; This guidance establishes a new hierarchy for determining the amount of arrangement consideration to allocate to each separable deliverable in an arrangement.&amp;#160; For those deliverables that qualify as separate units of accounting, the Company must assign value based on each deliverable&amp;#146;s&amp;#160; vendor-specific objective evidence (&amp;#147;VSOE&amp;#148;) of fair value if available, third-party evidence (&amp;#147;TPE&amp;#148;) of its value if VSOE is not available, or estimated selling price (&amp;#147;ESP&amp;#148;) if neither VSOE or TPE is available.&amp;#160; Arrangement consideration is then allocated to all deliverables using the relative selling price method.&amp;#160; The residual method of allocation is not permissible under the new guidance.&lt;/p&gt; &lt;p style='margin-top:0in;margin-right:0in;margin-bottom:6.0pt;margin-left:0in;text-indent:20.0pt;margin-left:.25in;text-align:justify;text-indent:.25in'&gt;In determining the separate units of accounting, management evaluates whether the delivered element has standalone value to the customer based on the consideration of the relevant facts and circumstances for each arrangement.&amp;#160; Factors considered in this determination include the customer&amp;#146;s research, development, production and product commercialization capabilities and the availability of these capabilities, as well as polymer development and manufacture expertise in the general marketplace.&amp;#160; In addition, the Company considers whether the customer can use the license for its intended purpose without the receipt of the remaining deliverables, whether the value of the license is dependent on the undelivered items and whether there are other vendors that can provide the undelivered item.&lt;/p&gt; &lt;p style='margin-top:0in;margin-right:0in;margin-bottom:6.0pt;margin-left:0in;text-indent:20.0pt;margin-left:.25in;text-align:justify;text-indent:.25in'&gt;Management performs extensive analysis to determine the value, or selling price, of each unit of accounting.&amp;#160; The Company has been unable to establish VSOE due to the fact that it does not typically enter into arrangements where technology is licensed separately, rather, its arrangements are commingled with fees from royalties, usage of polymers within customer end-products, minimum purchases of polymer products manufactured and sold to customers by the Company, or a combination of the aforementioned.&amp;#160; Additionally, the Company has been unable to obtain TPE for any of its deliverables, without undue cost and effort.&amp;#160; Generally, the Company&amp;#146;s go-to-market strategy differs from that of its peers and its offerings contain a significant level of customization and differentiation such that the Company&amp;#146;s services are not interchangeable with those of its competitors.&amp;#160; Furthermore, the Company is unable to reliably determine what similar competitor products&amp;#146; selling prices are on a standalone basis.&lt;/p&gt; &lt;p style='margin-top:0in;margin-right:0in;margin-bottom:6.0pt;margin-left:0in;text-indent:20.0pt;margin-left:.25in;text-align:justify;text-indent:.25in'&gt;Management&amp;#146;s ESP is used for the Company&amp;#146;s licensing, royalty and development arrangements.&amp;#160; The Company determines that ESP for the elements of these arrangements is based on several factors, including, but not limited to, the terms of the arrangements, market conditions, historical analysis of contracts having similar elements, and the Company&amp;#146;s internal costs and gross margin objectives.&amp;#160; The determination of ESP is made through consultation with and formal approval by the Company&amp;#146;s management.&amp;#160; ESP for certain consultative services is determined based on consideration of time incurred by the Company to perform these services, consulting fees charged on a per-hour basis by the Company and by its vendors, and the Company&amp;#146;s pricing methodologies.&lt;/p&gt; &lt;p style='margin-top:0in;margin-right:0in;margin-bottom:6.0pt;margin-left:0in;text-indent:20.0pt;margin-left:.25in;text-align:justify;text-indent:.25in'&gt;The Company&amp;#146;s arrangements generally do not include any provisions for cancellation, termination, or refunds that would significantly impact recognized revenue.&lt;/p&gt; &lt;p style='margin-top:0in;margin-right:0in;margin-bottom:6.0pt;margin-left:0in;text-indent:20.0pt;margin-left:.25in;text-align:justify;text-indent:.25in'&gt;In June 2011, the Company entered into a non-exclusive license agreement and a consulting services agreement (collectively, the &amp;#147;Agreements&amp;#148;) with a major international developer and manufacturer of medical devices (&amp;#147;Customer&amp;#148;), which generally provides the Customer the right to use and know-how to produce a specific proprietary polymer biomaterial for a specific field of use (the &amp;#147;Licensed Polymer&amp;#148;) within the Customer&amp;#146;s suite of medical device products.&amp;#160; In accordance with the applicable accounting guidance, the Company determined the Agreements included the following units of accounting:&amp;#160; (i) transfer of technology and know-how related to the Licensed Polymer, (ii) consulting services related to the establishment of a facility to manufacture the Licensed Polymer by the Customer, (iii) assisting the Customer in validating the Licensed Polymer produced by the Customer, and (iv) consulting with the Customer in connection with the Customer&amp;#146;s efforts to obtain various regulatory approvals for medical devices incorporating the Licensed Polymer.&lt;/p&gt; &lt;p style='margin-top:0in;margin-right:0in;margin-bottom:6.0pt;margin-left:0in;text-indent:20.0pt;margin-left:.25in;text-align:justify;text-indent:.25in'&gt;Upon the execution of the Agreements, the Company received an up-front payment of $150,000, and in July 2011, the Company received an additional $250,000 upon the transfer of technology and know-how related to the Licensed Polymer.&amp;#160; The Agreements also provide for additional payments upon the achievement of certain milestones, as previously described, each of which the Company considers substantive, and could total up to an additional $1,100,000.&amp;#160; The Agreements do not provide for any royalties or other fees upon the achievement of any or all of the milestones.&amp;#160; The Company determined that the transfer of technology and know-how of the Licensed Polymer represented a separate unit of accounting, and upon delivery, in accordance with the applicable accounting guidance, the Company recognized $400,000 of revenue during the fiscal year ended March 31, 2012.&amp;#160; During fiscal 2013, the Company achieved an additional milestone in connection with the functional installation of certain production equipment and recognized $20,000 of revenue during the fiscal year ended March 31, 2013.&lt;/p&gt; &lt;p style='margin-top:0in;margin-right:0in;margin-bottom:6.0pt;margin-left:0in;text-indent:20.0pt;margin-bottom:0in;margin-bottom:.0001pt;text-indent:0in'&gt;The adoption of this guidance resulted in an increase to revenue during the fiscal years ended March 31, 2013 and 2012 of $20,000 and $400,000, respectively, over the amount which would have been recognized under the principles used during the fiscal year ended March 31, 2011.&amp;#160; 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