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This 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 on the practice area page, which offers tools for drafting clinical research agreements. Users can access information on key topics such as contract research organizations (CROs) and IRBs. The practice note provides drafting tips for CRO agreements and links to precedents for benchmarking against public companies. It covers various agreement types, including clinical research support agreements, master clinical trial agreements, material transfer agreements, and sponsored research agreements.