We are ISO 21001 : 2018 Certified
We are ISO 21001 : 2018 Certified
Raaj GPRAC proud to EMPOWER Women’s for their second careers and helping to fill up Gaps in careers with Effective Training’s.
RAAJ GPRAC & Raaj Pharma eLearning was founded by Ms. Rajashri Survase Ojha in 2009-2010 and have been successfully completed 14 years as a Global CONSULTANT, TRAINERS & AUDITORS. We offer services into Pharma, Biotech/Biosimilars, Medical Devices, Nutraceuticals, OTC, Foods, and Veterinary.
We are based at Thane-Mumbai and providing services across the Globe [USA, EUROPE, CANADA, BRAZIL, ASEAN, BANGLADESH, MENA, GCC, ROW & ACROSS PAN INDIA]
Raaj Global Pharma regulatory Affairs Consultants (Raaj-GPRAC) is a premier training institute in Thane-Mumbai (India) offering comprehensive Regulatory Affairs services across the spectrum of product development, registration and commercialization.
Drug development proceeding to legally entry into market involves multiple steps which are completely governed and regulated by Global Health Authorities. Ensuring compliance throughout the process is a mandatory requirement and to overlook the procedures across the product life cycle, organizations deploy proven experts for Regulatory Affairs. We at RAAJ GPRAC acts as a crucial link between Organization and Global Health Authorities, tracking all the key regulations related to the product and pre-requisites for its launch.
RAAJ GPRAC is a leading Regulatory affairs services company and has been a pioneer in providing strategic multidisciplinary Regulatory affairs consulting services worldwide. We We are well-known for excellency, brilliance, stringent QA and QC standards, up-to-the-minute knowledge base, professionalism and unquestionable ethics.
Our channel is decked with latest updates and withstands huge capability in creating valuable facets, with a great experience of industry, creating a valuable package with utmost precision. We bring forth content and service which is customized to a client requirements and specifications.
Our knowledge of the laws and regulations pertaining to the development, testing, approval, manufacturing, commercialization and post-marking surveillance of a product provides you a good vantage point. Our focus is to acquire speedy approvals to enable clients achieve their objective of a timely and successful product launch.