Manufacture and Supply. With respect to the Territory, and except as may otherwise be specified in the Work Plan and Budget, Section 3.5, or any separate clinical supply agreement entered into by the Parties, Cempra shall, as between the Parties, be responsible for the manufacture of clinical materials for each Cempra Product, and for the commercial supply of each Cempra Product, and for all costs associated therewith. Cempra shall use Diligent Efforts to make necessary Regulatory Filings to obtain, or cause a Third Party manufacturer to obtain, Regulatory Approval in the Territory for the manufacture of Cempra Products.
Appears in 6 contracts
Samples: Collaborative Research and Development and License Agreement (Cempra Holdings, LLC), Collaborative Research and Development and License Agreement (Optimer Pharmaceuticals Inc), Collaborative Research and Development and License Agreement (Optimer Pharmaceuticals Inc)