Overcoming Site Regulatory Issues to Optimize Clinical Quality
PharmaTalkRadio11 Dec 2020

Overcoming Site Regulatory Issues to Optimize Clinical Quality

How two companies collaborated on a master trial to drastically improve site startup speed, reduce delays and optimize CRA productivity. In this podcast, Rick Arlow, Complion, and Dr Len Rosenberg, Leukemia and Lymphoma Society, discuss their collaboration on a LLS master trial, and how adopting Complion’s a purpose-built design optimized site functions and reduces startup time. Some specific discussion points included: The challenges sites face today with arduous manual tasksHow to pick the right point solution technology for your studyWhat the impacts of their collaboration have been on study progressHow this all benefits patients For more information about optimizing clinical research for the patient benefit and for improving care, visit the Clinical Research as a Care Option webpage. The 2021 Clinical Research as a Care Option event will be held April 26-28, virtually.

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