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This video tutorial demonstrates how to use the Practical Guidance Life Sciences practice area for preparing clinical research agreements related to drugs and medical devices. The clinical trials task on this page offers quick access to drafting tools and key information, including contract research organizations (CROs) and institutional review boards (IRBs). It highlights a practice note with drafting tips for CRO agreements and provides links to precedents of CRO and research services agreements for benchmarking with public companies. The resources assist in drafting various agreements such as clinical research support agreements, master clinical trial agreements, material transfer agreements, and sponsor agreements.