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Advanced Clinical Research: Regulatory Submission & Pharmacovigilance Strategies | AMSLC by CCRPS This lesson provides in-depth guidance on regulatory submission processes and pharmacovigilance strategies within clinical research. Designed for professionals pursuing clinical research certification, it highlights the critical role of accurate regulatory documentation, safety reporting, and risk management in live clinical trials. Learners will explore project management techniques for regulatory submissions, pharmacovigilance workflows, and strategies to ensure data integrity and compliance. This training aligns with real-world responsibilities of medical monitors, MSLs, CRCs, CRAs, and clinical trial managers, providing actionable insights for both site and sponsor settings. Part of CCRPS’s Advanced Medical Science Liaison & Medical Monitor Certification (AMSLC), this lesson contributes to a globally recognized, triple-accredited clinical research training program featuring live webinars, real case studies, toolkits, MCQs, and simulations. 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.