Master of Pharmacy (M.Pharm) in Drug Regulatory Affairs

Overview

The programme is designed to :

• Develop drug delivery system concepts based on biological, physicochemical and pharmaceutical approaches
• Strengthen their fundamentals and skills in analytical techniques
• Inculcate the GMP, GLP and Regulatory guidelines in pharmaceutical practices.

After completion of this programme, the graduate will :

• Design and investigate the drug based potential dosage form
• Analyze the approved API dosage form by different analytical techniques as per Regulatory guidelines
• Review the documentation, IPR issues and regulatory guidelines for pharma industry
• Determine biopharmaceutical parameters for existing dosage forms and establishing in vitro-in vivo correlation
• Select the excipients, production technology and instrumentation in the development of novel drug delivery system

Eligibility

Pass in B.Pharm degree from any university recognised as equivalent by RGUHS / PCI and AICTE with the minimum of 55% aggregate.

Minimum Education