Who We Are
A pharmaceutical consultancy built on decades of industry experience, ethical practice, and deep regulatory expertise.
RBridge Lifesciences Private Limited is a pharmaceutical consultancy firm specialising in GMP consulting, regulatory services, third party QP audits, technical due-diligence projects, and portfolio strategy. Our expertise extends to both regulated and emerging markets.
Our technical team consists of highly skilled professionals with extensive experience in the pharmaceutical industry, possessing up-to-date knowledge in GMP, regulatory affairs, portfolio strategy, product development, and project management.
Our goal is to establish ourselves as a trustworthy partner in regulatory, GMP, and due-diligence services — providing the industry with comprehensive, knowledge-driven, time-bound, and high-quality solutions.
Every recommendation is grounded in deep regulatory expertise and up-to-date knowledge of global health authority requirements.
We understand that regulatory timelines are business-critical. We commit to deadlines and deliver on them.
Compliance is not just our business — it is our standard. We operate with full transparency and professional integrity.
Leadership
Founder & Director
A Science Graduate with PG Diploma in Patents & IPR, Santosh brings over 33 years of regulatory affairs and quality compliance experience in the pharmaceutical industry. He is a BSI-certified Lead Auditor for ISO 13485 (Medical Devices) and has held senior leadership roles at Glenmark Pharmaceuticals, Alembic Pharmaceuticals, Emcure Pharmaceuticals, and Bluefish Pharmaceuticals AB (Sweden).
Since January 2018, he has operated as an independent GMP and regulatory consultant, trainer, and speaker at pharma conventions across India. He has personally conducted audits in India, Spain, China, France, and the UK, covering API, intermediate, and finished dosage form manufacturers.
He is also a visiting faculty member at the Pharmacy College of MIT WPU, Kothrud, Pune, and a guest speaker at Bharti Vidyapeeth Deemed University, Mumbai. He served as a panel member and speaker at Pharma Live Expo 2023 (NESCO, Mumbai) and was a committee member and speaker at IDMA PAC 2025 (December 2025).
Expert & Advisor
A result-oriented professional with 39+ years of experience in Quality Assurance and Quality Control, Savio has worked with organisations approved by USFDA, MHRA, TGA, Health Canada, ANVISA, WHO, INVIMA, CDSCO, and other international regulatory bodies. He has deep expertise in cGMP, QA systems, internal and external audits, CAPA management, and manufacturing compliance across global markets.
Expert & Advisor
A competent professional with 36 years of experience in Production Planning & Control, Quality Inspection, and Compliance. Well versed with ICH Q7A/Q8A and USFDA regulations, Ashok has handled USFDA, MHRA, EDQM, and WHO inspections. He brings expertise in technical due-diligence, safety audits, HAZOP studies, risk analysis, and ISO standards implementation. He has served as visiting faculty at NITIE, NSC, National Safety Council, and IIT Mumbai.
Expert & Advisor
A competent professional with 36 years of experience in Production Planning, P.D. Lab, and Production Compliance. Dr. Kolhe is well versed with WHO API regulations, FDA GMP, EU GMP Part II, and PIC/S API GMP regulations. He has handled USFDA, EDQM, WHO, and Mexico CGMP inspections, and brings extensive expertise in API process development, technology transfer, project management, and regulatory & GMP compliance.
Expert & Advisor
With 26 years of experience in Quality Control, Quality Assurance, and Analytical Development at Indian generic pharmaceutical manufacturers approved by USFDA, MHRA, TGA, WHO, and other PIC/S authorities, Vinayak brings hands-on expertise in inspection remediation, data integrity review, OOS investigation, GMP training, and analytical data review. He has been associated with GSK, Wockhardt, Megafine Pharma, and Harman Finochem as a consultant.
Get in touch to discuss your regulatory requirements.