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Aug 6th, 2022

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4.7 out of 5

22 votes

This video tutorial demonstrates using 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 an efficient way to access drafting tools and guidance. Users can find essential information on topics like contract research organizations (CROs) and institutional review boards (IRBs). The practice note offers drafting tips for CRO agreements and includes links to precedents that benchmark against public company agreements. The tutorial is useful for drafting various agreements, including clinical research support, master clinical trial, and material transfer agreements.

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