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This tutorial demonstrates how to use the Practical Guidance Life Sciences practice area for drafting agreements related to clinical research for drugs and medical devices. The Clinical Trials task within this area offers resources and tools focused on clinical trials, including information on contract research organizations (CROs) and institutional review boards (IRBs). A specific practice note provides drafting tips for CRO agreements, alongside links to precedents for CRO and research services agreements, enabling users to benchmark their documents against those of public companies. This guidance is intended to assist in drafting various agreements, including clinical research support agreements, master clinical trial agreements, and material transfer agreements.