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The tutorial demonstrates how to utilize the Practical Guidance Life Sciences practice area for preparing agreements related to clinical research on drugs and medical devices. To easily access tools for drafting clinical research agreements, users can visit the Clinical Trials task on the practice area page. It offers essential information on topics such as contract research organizations (CROs) and Institutional Review Boards (IRBs). The practice note provides drafting tips for CRO agreements and includes links to CRO and research services agreements precedents for benchmarking against public companies. It supports users tasked with drafting various agreements, including clinical research support agreements and master clinical trial agreements.