Regulatory Affairs and Drug Approval

Regulatory Affairs and Drug Approval focuses on the processes and policies governing the development, evaluation, and authorization of pharmaceuticals. This track will explore global regulatory frameworks, submission requirements, and approval pathways across major agencies like FDA, EMA, and others. Topics include compliance, clinical trial regulations, documentation standards, and post-marketing surveillance. Emphasis will be placed on aligning scientific innovation with regulatory expectations to ensure the timely delivery of safe, effective, and high-quality medicines to patients.

 

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