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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. Viewers can access fundamental information on contract research organizations (CROs), institutional review boards (IRBs), and other relevant topics. The tutorial also provides drafting tips for CRO agreements and offers links to precedents for benchmarking agreements against those used by public companies. It covers various agreement types, including clinical research support agreements, master clinical trial agreements, material transfer agreements, and sponsorship agreements.
