Master Of Pharmacy

Master Of Pharmacy (M-Pharma)

Master of Pharmacy (M.Pharm) is the standard Postgraduate Program in Pharmacy, Master of Pharmacy (M.Pharm) in India is offered as a Postgraduate course after the completion of B. Pharm degree. The M.Pharm is a two-year course. After completing M. Pharmacy, one can seek employment in government, private or multinational organizations. There are many opportunities in Chemical, Pharmaceutical, Biotechnology and allied industries. Some can be clinical analysts, quality supervisors or Scientists, researchers, work for government departments and educational institutions.

The M.Pharma has a research-based course curriculum that emphasizes the technical and practical aspects of the design and manufacture of medicines. The candidates are provided a strong foundation in the latest methods of production of medicines, different modes of drug delivery, product upgrade, analytical techniques, applications and dose selection. The M.Pharma is an interdisciplinary subject involving the application of chemistry, biology and technology in making drugs from natural and chemical substances, methods of delivering drugs into the body, positive effects and side-effects of drugs, and research for better improved medication.

Master Of Pharmacy (MPharm) is a two-year post-graduate program. The course is based on pharmaceutical sciences that deal with the study of drugs and medicines.

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

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