Common use of Responsibilities of the JDC Clause in Contracts

Responsibilities of the JDC. The JDC shall have the responsibility and authority to: (a) discuss, plan, revise and implement the Clinical Development Plan, including manufacturing of Irofulven for the Phase 2 Clinical Trial; (b) discuss, plan, and inform of any further Development of Products in all indications in the Field in the Territory, including manufacturing of Products in support of such activities; (c) use Commercially Reasonable Efforts to align each Party’s strategy for the Development of the Products in the Territory; (d) no less frequently than on a bi-annual basis, review, amend and approve any updates to the Clinical Development Plan, including the activities, budget and timeline for Development (see Section 4.2(b)); (e) review and approve proposed Publications in scientific journals, which will need to be approved unanimously by the JDC members, presentations at conferences, and/or press releases resulting from Development activities;