At the center of every clinical trial lies a maze of regulatory requirements, from FDA regulations to institutional review board (IRB) approvals, and improving compliance in clinical trials remains an imperative. For academic medical centers (AMCs), ensuring compliance with these regulations can be an overwhelming task, often requiring extensive paperwork, meticulous documentation, and stringent adherence ... Read moreThe post Improving Clinical Trial Compliance: Top 5 eRegulatory Features for Academic Medical Centers appeared first on RealTime-CTMS.
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