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Clinical Research Certification: Trial Phases 0–IV & Monitoring Procedures | AMSLC by CCRPS This lesson supports clinical research certification by explaining clinical trial phases 0 through IV and the monitoring procedures applied at each stage of drug and device development. As part of CCRPS clinical research training, it clarifies how trial objectives, risk profiles, and regulatory expectations evolve across early and late phases. Learners will examine phase-specific monitoring responsibilities, including protocol execution, safety oversight, data integrity, compliance checks, and communication with investigators and sponsors. The lesson connects clinical trials training to real-world workflows used by medical monitors, CRAs, and clinical trial leaders across sponsors, CROs, and global sites. Designed for physicians, medical monitors, MSLs, CRCs, CRAs, and regulatory professionals, this module emphasizes how monitoring intensity, safety reporting, and decision-making differ between exploratory, confirmatory, and post-marketing studies. These distinctions are critical for effective oversight, regulatory readiness, and patient protection throughout the trial lifecycle. This lesson is part of the Advanced Medical Science Liaison & Medical Monitor Certification (AMSLC) within CCRPS’s triple accredited clinical research training ecosystem. The program offers role-aligned curricula with structured lessons, real-world case analysis, live weekly webinars, applied assessments, and flexible learning formats for global professionals. This lesson is part of CCRPS’s role specific clinical research certification pathways, designed to match the day to day responsibilities of professionals working as CRCs, CRAs, pharmacovigilance specialists, project managers, and investigators across global trials. 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.