A Clinical Trial Agreement (CTA) is a critical legal document that defines the roles, responsibilities, and obligations between clinical trial sponsors and investigators. This template provides structured guidance to draft detailed agreements covering study scope, timelines, payment terms, confidentiality, data handling, intellectual property rights, and compliance with regulatory standards. It ensures clarity on risk management, indemnification, termination conditions, and dispute resolution, helping all parties align expectations and protect their interests. Use this template to create enforceable, professional CTAs that support successful clinical research collaborations.
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