Applications for Regulatory Approval. Clovis Oncology shall at its own expense be responsible for and control the preparation and submission of any applications for Regulatory Approval, and for obtaining and maintaining Regulatory Approvals, in the Territory for any Clovis Oncology Compound. RMS or its Affiliates shall be responsible for and control the preparation and submission of any applications for Regulatory Approval, and for obtaining and maintaining Regulatory Approvals, in the Territory for any IVD being developed in accordance with the Project Plan and this Agreement.
Appears in 2 contracts
Sources: Companion Diagnostics Agreement (Clovis Oncology, Inc.), Companion Diagnostics Agreement (Clovis Oncology, Inc.)