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Post Graduate Diploma In Drug Regulatory Affairs (Part Time)

The objective of PGD in Drug Regulatory Affairs program is to develop students...

The objective of Post Graduate Diploma in Drug Regulatory Affairs program is to develop students, over the period of 6 months, by in depth industry oriented knowledge to reach top end positions in the pharmaceutical regulatory affairs industries.

This program is developed and structured in a manner to match high academic standards and international regulatory industry requirements. The comprehensive syllabus of ICH Quality guidelines, eCTD submission, API and Formulation regulatory submission to developed and developing market along with workshop on Interview techniques, CV development ensure a fast successful corporate career.
We provide class room training with high quality presentations by our industrial expert trainers every Sunday.

Teaching Methodology

  • Classroom Lectures
  • Presentations
  • Assignments/ Project
  • International Level Certificate

Duration

6 Months- Every Sunday.

Students
  • Best Equipped Training Cente
  • Overall Development Through Academic Lectures + Presentation Skills + Interview Skills + CV Development
  • Free Study Material
  • Free Wi-Fi
  • Industry Oriented Training
  • Visiting Lectures by Expert Industry People
  • Placement Program
  • International Level Certificate

Batches : March & September Each Year

Syllabus

Final Written Exam Will Be Conducted and Certificate will Be Awarded to Successful Candidates Only.

Eligibility

B.Sc/M.Sc in Life Sciences / Microbiology / Biotechnology / Zoology / Biochemistry / Chemistry / Nursing

B.Pharm/ M.Pharm

BAMS/ BHMS/ BDS/ MBBS/ Physiotherapy.

ProRelix provides complete placement support to its students. Students will get continuous job placement support including job emails on their email IDs provided to ProRelix Lifesciences Education.

Type of companies hiring RA professionals: Pharmaceutical, Medical Devices, Biotechnology, Regulatory Authorities, Clinical Research Organization/ Contract Research Organization

  • Regulatory Affairs Associates
  • Regulatory Affairs Assistant
  • Regulatory Affairs head/ Director
  • Medical Information Associates
  • Drug Inspector
  • Drug Safety Specialist/ Regulatory Food Safety Scientist
  • Quality Operations/Quality Control/Quality Assurance
  • Regulatory Affairs Consultants

Companies enrolling clinical research candidates –
Cognizant Technology Solutions, Syntel, Jahangir Clinical Development Centre, JSS Medical Research, ACCESS Healthcare, Crest Healthcare, IT Cube Solutions, TCS, Sciformix, Lupin, Cipla, Tata Memorial Hospital, Quintiles, Covance, Accenture, Bioclinca, Freyer

September & March Each Year

FAQ

What is Post Graduate Diploma In Drug Regulatory Affairs?

A Post Graduate Diploma in Drug Regulatory Affairs covers all the topics pertaining to the pharmaceutical drug development process and how they are subject to various degrees of regulation in the market. Some of the topics that you will learn in this module are: ich gcp guidelines, international drug regulations, eCTD submission, and more.

Is Post Graduate Diploma In Drug Regulatory Affairs a good course?

A PG Diploma in Drug Regulatory Affairs is an exemplary choice for somebody who is interested to review the safety and efficacy of pharmaceutical products, medical devices, drug regulations, and etc. As there’s a large demand for trained professionals in this niche, it promises good career growth and many of job opportunities which make it a decent course to opt for!!

Benefits of pursuing a Post Graduate Diploma In Drug Regulatory Affairs course?

A “Post Graduate Diploma in Drug Regulatory Affairs” is a comprehensive course that revolves around the various aspects and phases of the pharmaceutical regulatory affairs industry. The course is designed to give students insights into the basics as well as the advanced topics such as ICH GCP guidelines, eCTD submission procedure, DMF composing, Dossier preparation and many more. The course focuses on the overall development of the students making them the ideal candidate for lucrative job roles.

Job opportunities after completing Post Graduate Diploma In Drug Regulatory Affairs?

A post-graduate diploma in Drug regulatory affairs can lead to a variety of exciting job opportunities both in India and abroad. Hands-on experience in the field is essential for a successful career in regulatory affairs. There is a constant demand for new medicines to cure a wide range of diseases, which raises the demand for trained professionals in the field of regulatory affairs.

Highlights

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Free Study Material

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Best Equipped Training Center

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Industry Oriented Training

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