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hi everyone we have scott laughlin in the hogan levels privacy group im excited to be joined by two councils on our team melissa levine and elizabeth mcguire to discuss trends and particular importance to our life science clients engaged in clinical studies having negotiated many clinical trial agreements in the past that can attest that their complexity creates many traps for the unwary and your article elizabeth and melissa focuses on one of those issues provisions regarding remote monitoring and so im curious elizabeth your article discusses how the pandemic has altered how sponsors are fulfilling monitor requirements maybe you can explain why uh sure scott so you know as you may know clinical trials sponsors are required to monitor the progress of the clinical trial this is a regulatory requirement from fda but historically monitoring of clinical trials was done by an in-person visit so the sponsor or their cro representative would go on site and review the clinical trial data b