What is the Master of Pharmacy [M. Pharm] (Drug Regulatory Affairs)?

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Master of Pharmacy [M. Pharm] (Drug Regulatory Affairs) is a four-semester regular postgraduate course that drives the Research and Development efforts of the pharmaceutical companies to the market. The minimum educational qualification for getting admission into the Master of Pharmacy [M. Pharm] (Drug Regulatory Affairs) course is a minimum aggregate score of 45% in B.Pharm from a recognized University. 

Drug Regulatory Affairs is a crucial component of the pharmaceutical industry as it increases global competitiveness among pharmaceutical companies. Master of Pharmacy [M. Pharm] (Drug Regulatory Affairs) is a 2-year full-time postgraduate course that aims towards a comprehensive education in gaining Regulatory and Quality Compliance in the pharmaceutical industry.


  • The admission to the Master of Pharmacy [M. Pharm] (Drug Regulatory Affairs) course is usually based on the marks obtained by the candidates in graduation or the performance in a relevant entrance test.

  • In India, the average tuition fee charged for the Master of Pharmacy [M. Pharm] (Drug Regulatory Affairs) course ranges between INR 72,000 and 5,20,000 for a span of 2 years.

  • The average annual salary offered to professionals with specialization in Master of Pharmacy [M. Pharm] (Drug Regulatory Affairs) ranges between INR 3.5 and 7 Lacs.


Such professionals who have earned a postgraduate degree in Master of Pharmacy [M. Pharm] (Drug Regulatory Affairs) are hired for different specialized roles such as:


  • Medical Information Associate

  • Regulatory Affairs Specialist

  • Regulatory Affairs Consultant

  • Regulatory Affairs Associate

  • Drug Safety Specialist

  • Quality control Associate

  • Food Safety Scientist

  • Drug Inspector/Drug Controller


Master of Pharmacy [M. Pharm] (Drug Regulatory Affairs) is a multi-dimensional course that specializes in medical professionals with the utmost proficiency in their core domain. The course covers a wide scope of medical regulations and several key areas of specialization as mentioned below:


  • Drug Safety Specialist

  • Regulatory Food Safety Scientist

  • Regulatory Affairs Director/Head

  • Regulatory Administrator

  • Regulatory Compliance Manager

  • Quality Operations

  • Quality Control

  • Quality Assurance

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