Vasantidevi Patil Institute of Pharmacy

vpip@yspm.in

(02328) 223341

NAAC

vpip@yspm.in

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VASANTIDEVI PATIL
INSTITUTE OF PHARMACY

HTML marquee Tag Vasantidevi Patil Institute of Pharmacy, Kodoli, has been accredited with an A Grade, achieving an impressive CGPA of 3.07 by NAAC.
HTML marquee Tag Vasantidevi Patil Institute of Pharmacy, Kodoli was established with the aim to impart quality pharmacy education and training to cater the needs of the pharmacy profession and society at large. The journey started in 2003 by introducing the first Pharmacy institute in the Kodoli under aegis of Shri Yashwant Shikshan Prasarak Mandal, Kodoli. The institute is approved by AICTE New Delhi, PCI New Delhi, and DTE Mumbai, recognized by Government of Maharashtra & affiliated to a MSBTE, Mumbai and Shivaji University, Kolhapur. The Institute is situated at the foot hills of Panhala, in the area of Kodoli, about 10 kilometres away from National Highway- 4 and 35 km away from major city, Kolhapur. The institute occupies the area of approximately 4 acres having its own 5470 sq.mts. building with excellent infrastructure which in-houses facilities such as sophisticated laboratories, resourceful library with latest books, national& international journals and well-equipped classrooms with modern teaching aid. Vasantidevi Patil Institute of Pharmacy is a progressive edifying organization, dedicated to the pursuit of excellence. This institute has been dedicated to decree solutions to big challenges and to prepare the student for leadership in a multifaceted world.
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M.Pharmcy (Quality Assurance Techniques)
Course PEO's, PO's, PSO's & CO's

Programme Educational Objectives (PEO)

  • Build an education leading to a Masters’ degree in Quality Assurance Techniques with integrated professional knowledge and skills in interpreting regulatory guidelines and practices in a changing regulatory environment.
  • Equip the Masters’ students with comprehensive knowledge and skills to deliver regulatory services in regulated, semi-regulated and poorly regulated markets.
  • Cultivate an inclination for higher education, consultancy, and entrepreneurship.
  • Foster the best in-class hands-on training in dossier submissions as per global standards.
  • Empower and sensitize the regulatory affairs professionals to serve the pharmaceutical industry, academia, society, and the business.

 Programme Outcome (PO) 

  • Demonstrate competency in the area of pharmaceutical quality systems, drug development research, and drug regulations.
  • Develop competency in quality related problem identification, analysis and solving.
  • Demonstrate competency in designing and using various quality tools for trouble shooting.
  • Implement knowledge for conducting audits and investigations on quality issues in every stage of drug development and manufacturing.
  • Demonstrate competency in implementing modern tools like Quality by Design (QbD), Process Analytical Technology (PAT), Design of Experiments (DoE), Technology Transfer etc.
  • Evolve as entrepreneurs in the pharmaceutical field to serve the society.
  • Comprehend the impact of pharmaceutical industry operations on the environment and strive to make the pharmaceutical manufacturing sustainable.
  • Inculcate a sense of fair play, social values, and professional ethics.
  • Cultivate a sense of compliant partnering collaborative spirit in professional duties; develop transdisciplinary approaches in the area of pharmaceutical sciences through choice / problem-based learning.
  • Conceptualize research ideas, develop oral and written communication skills including soft skills, frame and evaluate hypothesis by collating and interpreting data to draw meaningful conclusions.
  • Acquire skills in managing human, financial and other resources efficiently to achieve the project objectives and stake holder’s satisfaction.
  • Cultivate a temperament that would enable individuals to work towards self-driven performance-goals, entrepreneurial ventures, and overall leadership to tackle future challenges through lifelong learning and staying ahead of times.

Programme Specific Outcome (PSO)

  • Know the principles of quality assurance, Good Manufacturing Practices, Good Laboratory Practices, and its application in pharmaceutical industries.
  • Be able to interpret various spectroscopic and chromatographic data for qualitative as well as quantitative analysis of drug substances and drug product.
  • Know the fundamental concepts of Quality Control and Quality Assurance which is important to maintain quality and safety of pharmaceutical product.
  • Be able to execute a research project in Pharmaceutical Sciences leading to Ph. D. degree, Patent, Commercial product, or Services etc.