WORKSHOP ON REGULATORY REQUIREMENTS FOR MEDTECH STARTUPS
The goal of the R Clinic is to understand current regulatory requirements and roadmap for securing regulatory approval for medical products in India. The Clinic will also focus on understanding the relevant Acts/ Laws/ Rules and standards applicable to the respective drugs and medical devices.
Note: Startup companies (LLC/PLC) vs individuals if we receive more than 50 applications. Organizers reserve the right to select participants so as to optimize the group for better interaction and ensure benefit to as many startups possible. Registration closes once 50 seats are full or on 18th Feb 2019 (whichever comes sooner).
Target Beneficiaries:
Aspiring Medtech/Healthcare Startup Entrepreneurs
Innovators & Research Scholars
BIG Grantees
RESOURCE PERSONS
Dr Ravindra Ghooi
Director, Scientia Clinical Services Specialties: Clinical Research Consultation Setting up of CR academies Consultation in setting up IECs Upgrading clinics to trial sites.
Mr Navnath Kadam
Asst Manager, RIFC - Venture Center
Navnath regularly advises startups on planning their regulatory roadmap and facility planning. He is developing a suite of services and resources of use to startups. He has multifaceted working experience in managing Quality and Regulatory operations at Medical Device startup Axio Biosolutions Pvt Ltd.
Dr S Ramalingam
Dean, PSG Institute of Medical Sciences & Research & PSG Hospitals
He is also the Founder Chair of the Department of Clinical Research and Bioethics, and is a Professor of Pharmacology in the same Institute. Dr Ramalingam obtained an International Fellowship in Medical Education (IFME) offered by the ECFMG of USA.
