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This video tutorial demonstrates how to utilize the practical guidance life sciences practice area for preparing agreements related to clinical research for drugs and medical devices. It highlights the clinical trials task as a quick resource for drafting clinical research agreements. Users can access content concerning clinical trials fundamentals, including information on contract research organizations (CROs) and institutional review boards (IRBs). The tutorial also offers drafting tips for CRO agreements and provides links to precedents for benchmarking with public company agreements. It covers various agreement types such as clinical research support agreements, master clinical trial agreements, material transfer agreements, and sponsored research agreements.
