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Raaj Global Pharma Regulatory Affairs Consultants (RAAJ GPRAC)

RAAJ GPRAC & Raaj Pharma eLearning was founded by Rajashri Survase Ojha in 2009-2010 and have been successfully completed 14 years as a Global CONSULTANT, TRAINERS & AUDITORS. We offer services and training into Pharma, Biotech/Biosimilars, Medical Devices, Neutraceuticals, OTC, Foods, and Veterinary after having 34+ years of industrial experience from Sandoz, Ciba-Geigy, Local FDA, Glenmark, GSK-TCS, Novartis, Famycare, Pregna International, Cognizant, Spectrum Pharmatech, Synergy Pharma UAE, Paras Organics, Saitech,.

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Top and Intense Quality Content

In-depth content along with additional videos, resources, articles, live webinars, online sessions and reading materials

Highly Skilled Instructor

Highly Experienced and qualified instructor for each topic. You can chat, interact and clarify doubts with experts during the Q&A sessions

Get Professionally Certified

Receive a Certificate of Completion for each course after successfully passing the online exams.

Online education, Anywhere at anytime

Attend the e-Learning lectures from the comfort of your home. Experience the benefits of the physical program, via LMS

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Certified Courses

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YEARS OF EXPERTISE

TESTIMONIAL

What others say about us

I have found Regulatory Affairs Formulation course very helpful for gaining a better idea of what Regulatory Affairs is about. The material is clear and concise. It is easy to follow. Whenever I needed help then Raaj GPRAC was always ready to help me out with my questions and cleared my doubts...

Rishi Ratna Dewan

I am very grateful to have got the ppportunity to attend Medical Devices Course with Raaj GPRAC team. My expericence of joining Medical Device Regulations Course wirh Raaj GPRAC is very good. All the topics were well explained with real examples from Medical Device industry...

Nupur Pitkar

-Director, SAP function at S.H. Pitkar Orthotools Pvt.Ltd

I want to thank RAAJ GPRAC for everything and more so for the training. Hands on training and interaction with trainer and trainees on personal experiences related to regulatory Affairs was excellent...

Castro Wanjoya

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'PHARMA, BIOTECH, MEDICAL DEVICES Industry' Career

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Recent Post

  • 10 Jan, 2024
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All about Global Pharma Regulatory Affairs Online Certification Course

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  • 5 Feb, 2024
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Importance of Good Documentation Practices (GDocP) for Pharmaceutical and Medical Device Companies

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OUR

Recent Webinars

Online Training Anytime from Anywhere!!

MDD to MDR Implementation

  • Date: 7th and 8th May 2022
  • Time: 5:30pm to 9:00pm
  • Fees: Rs.10000+1180 (GST)=11800/-

Internal Auditor ISO 13485:2016 (QMS)

  • Date: 14th -15th May 2022
  • Time: 5:30pm to 9:00pm
  • Fees: Rs.10000+1180 (GST)=11800/-

MDSAP Webinar

  • Date: 21st -22nd May 2022
  • Time: 5:30pm to 9:00pm
  • Fees: Rs.10000+1180 (GST)=11800/-