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ICH GCP Review for Clinical Research Coordinators (CRC) | ACRCC by CCRPS Clinical research coordinator training requires a strong, working command of ICH GCP principles to ensure compliant clinical trial conduct. This lesson provides a focused ICH GCP review for Clinical Research Coordinators, reinforcing how Good Clinical Practice standards apply in real site-based trial environments. Delivered as part of the Advanced Clinical Research Coordinator Certification (ACRCC), this session reviews core ICH GCP E6 R3 concepts as they relate to CRC responsibilities, including protocol adherence, informed consent, source documentation, safety reporting, data integrity, and inspection readiness. The lesson emphasizes how GCP principles translate into day-to-day operational decisions at clinical trial sites. Learners will examine how CRCs support investigators, interact with monitors, and maintain compliance across study start-up, conduct, and close-out phases. The review connects regulatory expectations with practical execution, helping CRCs identify common compliance risks and apply GCP standards consistently during monitoring visits, audits, and regulatory inspections. Positioned within CCRPS’s triple accredited clinical research training ecosystem, this lesson supports professionals seeking structured, role-aligned GCP training that reflects real world clinical trial workflows. It is designed for CRCs and site professionals who require a clear, applied understanding of ICH GCP to perform confidently in global clinical research settings. CCRPS delivers globally recognized, triple accredited clinical research training aligned with CPD, ACCRE, CE, NHA, and TransCelerate standards. Our programs are designed to mirror real world clinical trial execution across sites, sponsors, CROs, and regulatory environments. Learn more: https://ccrps.org Explore programs: https://app.ccrps.org Call advising: +1 801 515 4867 Educational Disclaimer: ------------------------------------- The content provided on this channel is intended for educational and informational purposes only. CCRPS does not provide medical advice, clinical treatment recommendations, legal guidance, or professional services through this content. All information shared is based on general principles of clinical research, regulatory standards, and industry practices and should not be considered a substitute for professional judgment, institutional policies, or regulatory requirements. Viewers are encouraged to consult qualified professionals, official guidelines, and regulatory authorities before applying any information in clinical, research, or professional settings. CCRPS assumes no responsibility for actions taken based on the content presented in these videos.