New Delhi: To unleash the potential of the sector and brainstorm the path ahead, the Department of Pharmaceuticals, Ministry of Chemicals & Fertilizers, Government of India is hosting the pioneering ‘INDIA MEDTECH EXPO’ with central theme ‘India: The Next MedTech Global Hub’ Future of Devices, Diagnostics and Digital’, which is being organized alongside G20 Health Ministers’ Conference.
The Expo will have various pavilions, including Future Pavilion, R&D Pavilion, Start-up Pavilion, State Pavilion, Regulators Pavilion and Make in India Showcase. More than 400 exhibitors including 150 plus MSMEs, 150+ Domestic and International Manufacturers, Start-ups, Regulatory agencies, State Governments and Central Departments will participate in it.
As many as 7 States – Madhya Pradesh, Tamil Nadu, Uttar Pradesh, Himachal Pradesh, Rajasthan, Andhra Pradesh and Gujarat are setting up pavilions during the expo.
The expo will have pavilions for Innovations and R&D, wherein more than more than 30 companies will showcase new research and innovations. A separate pavilion for Start-ups will also be there and as many as 75 Start-ups are participating in it.
Further, 7 regulatory agencies for Medical Devices Sector including Department of Pharmaceuticals, GeM, ICMR, IPC, CDSCO, NPPA and BIS are participating in it.
In addition to that, thematic Conference Sessions will be organised during the 3-day event, with the aim to explore boundless frontiers of knowledge, inspire innovations, and forge connections that transcend boundaries. The Thematic Conference Sessions are created keeping aim of achieving Vision 2047, a vision that embodies India’s aspirations for the MedTech sector, not just within India but also as a significant contributor to the global healthcare landscape.
Through the 3-day conference, the event aims to:
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Bring together professionals, experts, and innovators from various fields to discuss the latest advancements, challenges, and opportunities in the medical device sector.
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Renowned industry leaders and experts will share their insights and experiences, shedding light on the current trends and prospects in the medical device domain.
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Latest regulatory guidelines and compliance requirements to ensure successful product development and market access will be discussed among Industry leaders and Policy makers.
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Thought-provoking discussions with industry experts, regulators, and healthcare practitioners about the challenges and opportunities in medical device development, regulation, and implementation.