Modern Pharmacovigilance in the Mobile Health Era | Clinical Research Certification
This lesson supports clinical research certification by examining proactive pharmacovigilance approaches in the mobile health era. It is designed for professionals responsible for safety surveillance, digital data integration, and regulatory oversight in modern clinical trials and post-marketing environments.
As part of advanced clinical research training, this module explores how mobile health technologies, digital reporting tools, and real-world data sources are reshaping pharmacovigilance practices. Learners gain insight into proactive safety monitoring models, continuous signal detection, patient-reported outcomes, and the regulatory considerations associated with mobile and decentralized safety data collection.
The lesson connects emerging trends to real-world responsibilities such as safety reporting workflows, data quality management, regulatory compliance, and cross-functional collaboration between sponsors, CROs, and technology partners. It highlights how proactive pharmacovigilance supports earlier risk identification, improved patient safety, and inspection-ready safety systems in global clinical trials.
This content is delivered within the Advanced Pharmacovigilance & Regulatory Affairs Certification (APVASC) program and is relevant for pharmacovigilance professionals, regulatory specialists, clinical research associates, and clinical trial leaders seeking globally aligned clinical research certification pathways that reflect evolving digital trial environments.
CCRPS training emphasizes applied clinical research execution through real case scenarios, regulatory documentation, monitoring workflows, and compliance driven decision making to help professionals perform confidently in live trial environments.
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Educational Disclaimer:
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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.
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