RAAJ

Raaj GPRAC PVT LTD

@raj_gprac

Thane-Mumbai, Maharashtra
http://www.raajpharmaelearning.com
Pharmaceutical Manufacturing

Overview

About Raaj GPRAC PVT LTD

Established in 2009-2010 by industry veteran Rajashri Survase Ojha, Raaj GPRAC & Raaj Pharma eLearning has earned a reputation as a premier global consultancy and training institute. With over 27 years of expertise in leading organizations like Sandoz, GSK, Novartis, and Cognizant, we deliver world-class solutions across Pharma, Biotech, Medical Devices, Nutraceuticals, OTC, Foods, and Veterinary sectors.

Our Core Services Include:

Comprehensive GMP, GLP, GCP, GDP, and Regulatory Compliance support
Globally recognized Pharmaceutical Training Programs (Classroom & Distance Learning)
Why Choose Us?

Accreditations: Certified by ISO 29993:2017 and accredited by the Life Sciences Sector Skill Development Council (LSSSDC) under NSDC (Government of India).
Global Reach: Successfully trained over 11,500 professionals across the world.
Career Advancement: Our training equips both fresh graduates and seasoned professionals to excel in their careers, with alumni securing prominent roles in the industry.
Tailored Programs for Diverse Professionals:
We offer a wide range of fast-track and specialized courses for individuals from diverse educational and professional backgrounds, including B.Pharm, M.Pharm, PhD, B.Tech, M.Tech, B.Sc, M.Sc, Biotech, BAMS, BHMS, BDS, MBBS, MD, and professionals in Regulatory Affairs, Quality Assurance, and Clinical Research.

Our flexible learning models—Weekend Classroom Programs and Distance Learning Courses—are designed to meet the needs of busy professionals and students alike.

Join us to gain the advanced skills and knowledge needed to succeed in the dynamic life sciences industry.

Visit us: www.raajpharmaelearning.com

Headquarters

Thane-Mumbai, Maharashtra

Website

http://www.raajpharmaelearning.com

Company Size

11-50 employees

Industry

Pharmaceutical Manufacturing

Company Type

Self-Owned

Founded

2010

Specialties

Regulatory Affairs, Compliance and submissions in CTD/eCTD to different Health Authorities., Audits and Compliance , Trainings, Validations, Medical Writing, Pharmacovigilance, DMF Applications, Dossier writing, Quality Systems, Pharma Management, NUTRACEUICAL, MEDICAL DEVICE, and BIOSIMILARS

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