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This video tutorial demonstrates how to use the Practical Guidance Life Sciences Practice Area to prepare agreements for clinical research related to drugs and medical devices. It highlights the Clinical Trials task as a quick resource for drafting clinical research agreements. Users can access fundamental information about contract research organizations (CROs), institutional review boards (IRBs), and related issues. The practice note offers drafting tips for CRO agreements and provides links to precedents for benchmarking against public company agreements. The tutorial covers various types of agreements, including clinical research support agreements, master clinical trial agreements, material transfer agreements, and sponsor agreements.