Sandip Phadatare

Regulatory Affairs Manager (Medical Devices)/ISO 13485 Lead auditor/EU MDR/IVDR/PRRC/510K/NBO/CDSCO Licensing/Aundit preparation and handeling/In country Registraion

Role: Regulatory Affairs Manager at Cipla
Location: Pune Division, MH, IN
LinkedIn followers: 500 followers

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About Sandip Phadatare

Having 7+ years of experience in medical device industry. Preparation of Technical…

Experience

Regulatory Affairs Manager
Cipla
Feb 2022 — Present · Mumbai, IN

Contact information

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Current company

Cipla

Pharmaceutical Manufacturing · 52K employees · Mumbai, India

Cipla is a leading global pharmaceutical company trusted by healthcare professionals and patients across the world since 1935. A compassionate approach to healthcare that goes beyond the pursuit of profit and growth has been the force impelling Cipla’s history over the years. Our credo and our purpose of ‘Caring for Life' continues to guide our actions towards our people and the planet for creating a sustainable future. Cipla today has presence in 80+ countries, providing over 1,500 products across various therapeutic categories in 50+ dosage forms. Keeping with our legacy of care, we constantly strive to ensure access to high-quality medicines that make a difference in the lives of patients. Our paradigm-changing offer of a triple anti-retroviral (ARV) therapy in HIV/AIDS at less than a dollar a day in Africa in 2001 was pivotal in bringing inclusiveness, accessibility and affordability to the centre of the HIV movement. An unmatched presence across the care continuum (awareness, prevention, diagnosis, treatment and adherence) and the widest range of drug-device combinations has established Cipla’s respiratory leadership in India and other key emerging markets. Armed with this legacy and a deep understanding of the lungs, we have articulated our aspiration to become a global lung leader and help millions breathe free.

cipla.com

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