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In this video, Scott Laughlin introduces a discussion with counselors Melissa Levine and Elizabeth McGuire about trends important to life science clients in clinical studies. They highlight the complexities of clinical trial agreements, which can lead to potential pitfalls. Elizabeth's article focuses on how the pandemic has changed the monitoring process for clinical trials, a regulatory requirement by the FDA. Traditionally, monitoring involved in-person visits by sponsors or CRO representatives to review trial data on-site. The pandemic has necessitated a shift in these practices.