Department of Pharmaceutical Analysis and Quality Assurance

Department of Pharmaceutical Analysis and Quality Assurance

Analysis of drugs and pharmaceutical formulations is the backbone of research and development in pharmaceutical industry. Pharmaceutical Analysis & Quality Assurance is a broad subject area that includes qualitative and quantitative analysis of drugs, excipients, impurities etc. to meet the regulatory requirements.

M. Pharmacy is a two year academic course.

Specializations & Intake

  1. Pharmaceutics (18)
  2. Pharmaceutical Analysis & QA (18) 
  3. Pharmaceutical management & Regulatory Affairs (18)
Eligibility

Candidates who have passed in B. Pharmacy Degree from any AICTE (All India Council for Technical Education) recognized College/ University with not less than 50% of the Maximum Marks (Aggregate of 4 years in B.Pharmacy). Admission is made through GPAT and/or PGECET for A-Category  Seats.

Objectives

To produce a competent pharmaceutical analyst to meet the demands of the pharmaceutical industries in terms of analysis, control of materials (raw and finished), standards and compliance with regulatory bodies and also to develop ability to work in pharmaceutical industries on modern analytical methods, instruments, analytical method development, validation, analytical research and achieving global standards.

Research Centre

Our institute has excellent research facilities in the various fields of pharmaceutical sciences. This institute has state-of-art analytical instruments like HPLC, UV spectrophotometer, FT-IR spectrophotometer etc. which provides analytical support and intellectual input to both in-house and externally funded R&D projects.

Career Prospects

After the completion of master degree in Pharmacy (Pharmaceutical Analysis & Quality assurance), one will have good range of career options in various pharmaceutical and chemical companies, in the departments concerning Analytical R&D relating to Formulation and API, Quality control and Quality assurance, Validation, TTG (technology transfer group), Regulatory Affairs.

Specific Features

  • Regular Guest Seminars from Industry & Institutional Professionals


  • In-house Projects
  • Industrial Visits
  • Practical Oriented Workshops
  • Conducting and Participation in National & International Seminars