Common use of Joint Development Committee Clause in Contracts

Joint Development Committee. As of the Effective Date, the Parties have established a joint Development, Medical Affairs, and regulatory committee (the “Joint Development Committee” or the “JDC”), composed of up to [ * ] representatives of each Party, to monitor and coordinate the Development of, and Medical Affairs Activities connected with, the Compound and Products at the operational level. Each JDC representative shall have knowledge and expertise in the clinical development of products similar to the Products. The JDC shall in particular:

Appears in 6 contracts

Samples: Collaboration and License Agreement (Exelixis, Inc.), Collaboration and License Agreement (Exelixis, Inc.), Collaboration and License Agreement (Exelixis, Inc.)

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Joint Development Committee. As of Within [***] after the Effective Date, the Parties have established shall establish a joint Development, Medical Affairs, and regulatory development committee (the “Joint Development Committee” or the “JDC”), composed of up to [ * ] representatives one (1) representative of each Party, to monitor guide the collaboration of the Parties under this Agreement and coordinate to oversee the exchange of information between the Parties with respect to the Development of, of Proprietary Drugs and Medical Affairs Activities connected with, Licensed Products until the Compound and Products at end of the operational levelfirst Phase 3 Clinical Trial for any Licensed Product. Each JDC representative shall have appropriate knowledge and expertise in and sufficient seniority within the clinical development applicable Party to make decisions arising within the scope of products similar to the ProductsJDC’s responsibilities. The JDC shall in particular:

Appears in 2 contracts

Samples: License Agreement (Dermavant Sciences LTD), License Agreement (Dermavant Sciences LTD)

Joint Development Committee. As of Within [***] after the Effective Date, the Parties have established shall establish a joint Development, Medical Affairs, and regulatory committee development team (the “Joint Development Committee” or the “JDC”), composed of up to [ * [***] representatives of each Party, to monitor and coordinate the Development of, and Medical Affairs Activities connected with, the Compound and Products at the operational level. Each JDC representative shall Party that have knowledge and expertise in the clinical development of products constructs similar to the Collaboration Products, with at least one member from each Party having Development decision-making authority, to monitor the Development of Collaboration Products. The role of the JDC shall in particular:be to oversee, monitor, and discuss the Development of such products and therapies.

Appears in 1 contract

Samples: Collaboration and License Agreement (Xencor Inc)

Joint Development Committee. As of Promptly after the Effective Date, the Parties have established shall establish a joint Development, Medical Affairs, and regulatory development committee (the “Joint Development Committee” or the “JDC”), composed of up to [ * [***] representatives of each Party, to monitor review and coordinate discuss the Development of, and Medical Affairs Activities connected with, the Compound of Compositions and Products in the Field in the ALFRESA Territory (and if applicable pursuant to Section 3.3, outside the ALFRESA Territory for the purpose of Regulatory Approval in the ALFRESA Territory), at the operational level. Each JDC representative shall have knowledge and expertise in the clinical development of products similar to the Products. The JDC shall in particular:

Appears in 1 contract

Samples: Collaboration and License Agreement (Silverback Therapeutics, Inc.)

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Joint Development Committee. As of Promptly after the Effective Date, the Parties have established shall establish a joint Development, Medical Affairs, and regulatory development committee (the Joint Development CommitteeCommittee ” or the “JDC“ JDC ”), composed of up to [ * ] three (3) representatives of each Party, to monitor review and coordinate discuss the Development of, and Medical Affairs Activities connected with, the Compound of Compounds and Products in the Field in the MTPC Territory (and if applicable pursuant to Section 4.3, outside the MTPC Territory for the purpose of Regulatory Approval in the MTPC Territory), at the operational level. Each JDC representative shall have knowledge and expertise in the clinical development of products similar to the Products. The JDC shall in particular:

Appears in 1 contract

Samples: Collaboration and License Agreement (Neurocrine Biosciences Inc)

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