Executive Development Programme Antiviral Drug Regulatory Affairs
-- ViewingNowThe Executive Development Programme in Antiviral Drug Regulatory Affairs is a certificate course that equips learners with the essential skills needed for success in the pharmaceutical industry. This program emphasizes the importance of antiviral drug development, a critical area in today's rapidly changing healthcare environment.
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โข Antiviral Drug Basics
โข Regulatory Landscape for Antiviral Drugs
โข Drug Development Stages and Regulatory Requirements
โข Clinical Trials Regulation and Compliance
โข Pharmacovigilance and Adverse Event Reporting
โข Chemistry, Manufacturing, and Controls (CMC) Regulations
โข Labeling, Packaging, and Prescribing Information Requirements
โข Data Integrity and Submission in Antiviral Drug Regulatory Affairs
โข Post-Marketing Surveillance and Monitoring
โข Regulatory Inspections and Compliance Audits
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