Jss College Of Pharmacy, Mysore

Jss College Of Pharmacy, Mysore

Description

The M. Pharm in Pharmaceutical Regulatory Affairs is a first time course offered in India introduced by JSS University. It aims to provide a comprehensive education in the important aspects of Regulatory and Quality Compliance in the pharmaceutical industry. Students are encouraged to enhance their knowledge of regulatory and compliance issues and to explore carets in these exciting times. The ever-changing laws and regulations are driving demand for pharmaceutical regulatory affairs professionals, who can help companies effectively bring medical products to market.

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...to know process of drug discovery and development and generic product development process and procedures for conducting clinical trials and its importance... Learn about: Pharmacy Research...

  • Master
  • Mysore
  • 24 Months
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Rs 4,00,000
VAT not incl.

History

JSS University, Mysore
Jagadguru Sri Shivarathreeshwara (JSS) University is established in 2008 under Section 3 of the UGC Act 1956. JSS Medical College, JSS Dental College and JSS College of Pharmacy in Mysore and JSS College of Pharmacy in Ootacamund of Tamil Nadu, are the constituent colleges of the university.
JSS College of Pharmacy, Mysore
JSS College of Pharmacy, Mysore is established in the year 1973 and is offering B.Pharm, Pharm D, and M.Pharm & PhD Programmes in Pharmaceutical Sciences. The college is accredited by National Board of Accreditation (NBA) and is also certified by ISO 9001-2008. The college is committed to provide quality education and research.

Advantages of studying here

Scope: This course is designed to impart the fundamental knowledge on the regulatory requirements for approval of new drugs, drug products, medical devices, biological, biosimilar, herbal products and nutraceuticals in regulated countries like US, EU, Japan, Australia, UK and Canada. It prepares the students to learn in detail on the regulatory requirements, documentation requirements, and registration procedures for marketing the drug products in regulated countries.

Objectives: Upon completion of the course, the student shall be able to know
• process of drug discovery and development and generic product development
• process and procedures for conducting clinical trials and its importance
• regulatory approval process and registration procedures for drug products in US, EU, Japan, Australia, UK and Canada
• regulatory approval process for Medical Devices, In vitro Diagnostics, biologics, biosimilars, herbal products and nutraceuticals in US and EU

Areas of specialisation

1. Pharmaceutical Quality Management
2.Pharmaceutical Regulations in India
3.International Pharmaceutical Regulations
4.Pharmaceutical Regulations in ROW Countries