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This video tutorial demonstrates how to utilize the Practical Guidance Life Sciences practice area for drafting agreements related to clinical research for drugs and medical devices. It highlights the Clinical Trials task as a quick resource for finding tools tailored to clinical trials. Key topics include contract research organizations (CROs), institutional review boards (IRBs), and associated matters. The tutorial provides drafting tips for CRO agreements and links to precedents for research services agreements, allowing users to benchmark their agreements against those of public companies. It addresses various agreement types, including clinical research support agreements, master clinical trial agreements, and material transfer agreements.