Classroom Cum Internship Program

Advance P G Diploma in Drug Regulatory Affairs - Full Time

Global Institute of Regulatory Affairs
In Pune

Rs10001-20000
You can also call the Study Centre
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Important information

  • Post Graduate Diploma
  • Pune
  • Duration:
    Flexible
  • When:
    Flexible
  • Credits:
Description

This course is designed to give industry level education in field of legal and regulatory issues. These issues are very critical to Pharma companies, Clinical Research Organization, Bio Tech companies. The course focuses on regulatory affairs concept which the Pharma companies must comply to sell their drugs both domestically and in the international market.

Important information
Venues

Where and when

Starts Location Timetable
Flexible
Pune
Prestige Classic BLD - Dwing Off no G4 & 5, CHinchwad station Chinchwad Pune, 411019, Maharashtra, India
See map

Frequent Asked Questions

· What are the objectives of this course?

Graduates in any stream of science are eligible to apply. Final Year Students can also apply.

What you'll learn on the course

Regulatory Affairs Associates
Regulatory Affairs head/ Director
Medical Information Associates
Drug Inspector/Drug Controller
Regulatory Affairs Consultants

Teachers and trainers (1)

Global Institute of Regulatory Affairs
Global Institute of Regulatory Affairs
Drug Regulatory Affairs

Course programme

Course Objective

    • To create a thorough understanding of important regulatory concepts
    • To create experts in the field of RA documentation and research.
    • To create an entry platform in the field of RA for fresh graduates.
    • To help students build their career in RA and become RA professionals.
    • To provide students with a global knowledge of Regulatory Affairs.

Course StructureTop

    • The Aims & Structure of Regulation
    • Regulatory Strategy
    • Marketing Authorization
    • Non – Clinical Studies
    • Clinical Trials
    • Good Manufacturing Practice (GMP)

Course DurationTop

    • 6 Months Full Time Class Room Program.

Learning OutcomeTop

    • Able to write Regulatory Documents
    • Create Regulatory Strategy
    • Get Marketing Authorization from different countries
    • Become an RA professional

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