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Course Name: Advanced Clinical Research, Regulatory Affairs & Pharmacovigilance

Course Description: Detailed study of clinical trial phases, FDA/CDSCO compliance guidelines, pharmaceutical safety tracking systems, drug dossier filing formats, and healthcare quality audits.

• Post-Course Benefits:
• Step into specialized roles like Regulatory Affairs Associate or Pharmacovigilance Officer.
• Understand strict local and global legal requirements for drug manufacturing and deployment.
• Master standard reporting tools used globally for tracing and evaluating drug safety signals.