Product Development and Commercialization Sample Clauses

Product Development and Commercialization. 13.1 XXXXXXX'X DEVELOPMENT RESPONSIBILITIES. Xxxxxxx shall be solely responsible for and have the sole right to select a compound for development into a Product. Once such a compound is selected for development, Xxxxxxx shall be solely responsible for and shall have the sole right to develop such compound throughout Pre-phase I and Phases I, II and III including making all Drug Approval Applications and obtaining all Regulatory Approvals on a worldwide basis. In this regard, Xxxxxxx agrees to carry out development of such compound consistent with its normal business practices. This development effort shall include the right to slow or terminate development and all other actions deemed by Xxxxxxx to be reasonable in the development of the compound. Moreover, Xxxxxxx shall be responsible for all cost and expenses in connection with such development efforts.
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Product Development and Commercialization. Within thirty (30) days ----------------------------------------- following the delivery of DTI's Notice of Election for a Co-Promoted Product, the parties will each appoint two (2) representatives as members of a "Product Committee" (the "Product Committee"). Within three (3) months after delivery of DTI's Notice of Election, such Product Committee will begin drafting the initial development plan for the subject Co-Promoted Product (the "Development Plan"). The parties shall request the Committee to complete such Plan no later -------------------------------------------------------------------------------- * Certain information on this page has been omitted and filed separately with the Securities and Exchange Commission. Confidential treatment has been requested with respect to the omitted portions. --------------------------------------------------------------------------------
Product Development and Commercialization. Firmenich, upon execution and for the duration of this Agreement, will diligently proceed with the evaluation of Compounds and the development, manufacture, marketing and sales of Products as set forth below.
Product Development and Commercialization. 5.1 In General. GSK, at GSK's sole expense (subject to ALLERGAN's performance of its obligations as set forth in Article 4 and Exhibits G and H), will use Commercially Reasonable Efforts to commercialize Product in the Territory, as provided in Section 5.5. Additionally, as provided in Section 5.3, GSK will develop Product for at least one (1)
Product Development and Commercialization. As of the Effective Date and during the Term, Orexigen will have full control, authority and responsibility over research, development, registration, manufacture, commercialization, marketing and sale of all Licensed Product in each country in the Field in the Territory, and all such activity will be undertaken at Orexigen’s sole expense and discretion.
Product Development and Commercialization. 34 5.1. General .................................................................................................................. 34 5.2. Regulatory Approvals ........................................................................................... 34 5.3. Commercialization Activities ............................................................................... 34 5.4. Manufacturing ....................................................................................................... 34 5.5. Reporting............................................................................................................... 34 5.6.
Product Development and Commercialization. (a) MERCK agrees to use commercially reasonable efforts, consistent with the usual practice followed by MERCK to take compounds forward within Merck Research Laboratories as drug development candidates, to take Active Compound(s) forward for approval as Program Compound(s). After MERCK’s approval of such a Program Compound, MERCK shall, at it own expense, use reasonable efforts to develop and to introduce a Product in a Major Market as soon as practical, consistent with the efforts MERCK uses in pursuing the development of other products representing a similar marketing opportunity. MERCK shall be deemed to have satisfied its obligations under this Section 3.3 if MERCK has an ongoing and active research program or marketing program as described above, as appropriate, directed in good faith toward production and use of a Product.
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Product Development and Commercialization. As of the Effective Date and during the Term, Orexigen will have full control, authority and responsibility over research, development, registration, manufacture, commercialization, marketing and sale of all Licensed Product in each country in the Field in the Territory, and all such activity will be undertaken at Orexigen’s or its Sublicensee’s or Further Sublicensees’s sole expense and discretion. *** Certain information on this page has been omitted and filed separately with the Commission. Confidential treatment has been requested with respect to the omitted portions.
Product Development and Commercialization. 16 6.1 LICENSEE'S Development Obligations; Product Development Plan. 16
Product Development and Commercialization. Within [...***...] of Ajinomoto’s first selection of an Ajinomoto [...***...] Compound, Ajinomoto shall provide Senomyx with [...***...] of Ajinomoto [...***...] Compounds, including plans for Ajinomoto [...***...] Product development, manufacturing and consumer acceptance testing. Ajinomoto will provide, at each Steering Committee meeting or if such meetings are no longer taking place, then on a [...***...] basis, [...***...] reports to Senomyx, which will include, without limitation, [...***...] of any Ajinomoto [...***...] Compound. Such reports will be treated as Confidential Information of Ajinomoto. Ajinomoto will use commercially reasonable efforts to obtain Regulatory Approval for [...***...]
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