Many site personnel, upon assuming responsibility for a new eRegulatory system, may not immediately recognize that, in addition to managing access credentials, the U.S. Food and Drug Administration now requires compliance with the guidelines outlined in the owner’s manual, specifically addressing electronic records and signatures as per 21 CFR Part 11 in the Code of Federal Regulations.
Topics highlighted include diversity and inclusion, decentralized clinical trial (DCT) elements, workforce challenges, and a possible role for sponsors and contract research organizations (CROs) in supporting outreach by sites based in diverse communities.
As Elisa Cascade, MBA, Chief Product Officer for Advarra, begins her volunteer duties as the 2024 Chair of the Association Board of Trustees (ABoT) for ACRP, she took time to answer some questions about her experience in the clinical research enterprise, some of the challenges facing it, and how ACRP can help to address them.
The Association of Clinical Research Professionals (ACRP) is pleased to announce that the following individuals have been elected by the ACRP membership to serve on the Association's Board of Trustees for 2024.
Health Care Compliance Association®(HCCA®) invites you to join us for our 28th Annual Compliance Institute, April 14–17 2024, where you can connect with other healthcare professionals and get the latest information and updates on healthcare compliance priorities and best practices.