Development; Manufacturing; Distribution; and Sale of Product. (i) Relypsa shall be solely responsible for all activities relating to the support for, or conduct of, any pre-clinical or clinical studies for the Product in the Territory, including post-approval studies, investigator initiated studies, health economics and outcomes/research, and phase 4 clinical studies. Costs and expenses for the foregoing activities shall be [***].
Appears in 4 contracts
Samples: Detailing Agreement, Detailing Agreement, Detailing Agreement (Relypsa Inc)
