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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. The Clinical Trials task on the practice area page offers resources for drafting clinical research agreements. It includes fundamental information on contract research organizations (CROs), IRBs, and provides drafting tips specifically for CRO agreements. Additionally, there are links to CRO and research services agreement precedents, useful for benchmarking against public companies. The resources can assist in drafting various agreements, including clinical research support agreements, master clinical trial agreements, material transfer agreements, and sponsor agreements.