About Conference
The medical device industry is at an inflection point. AI-enabled diagnostics, Software as a Medical Device (SaMD), cybersecurity mandates, and sweeping regulatory reforms are simultaneously reshaping how devices are designed, approved, and commercialized across every major market.
Now in its 3rd edition, Global MedTech Connect is India’s most focused executive platform for the medical devices and diagnostics sector. Held alongside the flagship India Health Exhibition at Bharat Mandapam, the summit convenes regulators, industry leaders, innovators, and policy architects for two days of high-signal, decision-grade dialogue.
The 2026 edition arrives at a pivotal moment: India’s MedTech market is projected to reach USD 50 billion by 2030, a government-backed manufacturing push via PLI schemes and dedicated MedTech Parks is reshaping the production landscape, and the industry is navigating import dependency, regulatory complexity, and the race to global harmonization - all at once.
This is not a conference built for awareness. It is built for action, equipping senior professionals with the regulatory clarity, market intelligence, and strategic connections needed to move faster and more confidently in a high-stakes environment.
Speakers
General Manager - MedTech
Zydus MedTech
Managing Director
FUJIFILM Sonosite India
Head - Regulatory Affairs
Edwards Lifesciences
Senior Director, Quality and Regulatory Affairs
Fresenius Medical Care
Advisor & Head, Public Health Administration
National Health Systems Resource Centr
President-Global Govt Affairs
Meril
Global Service Line Manager MHS - Cyber Security
TÜV SÜD
Asst. Vice President - MHS
TÜV SÜD
Vice President, External Affairs (Policy, Govt Relations & Outreach)
Sahajanand Medical Technologies
Agenda
Agenda
Key Features
From Innovation to Impact: Building a Trusted, Connected & Intelligent MedTech Ecosystem
Securing the Device Lifecycle - From Design to Post-Market Monitoring in Connected Healthcare Systems
Panel Discussion: Regulation vs Innovation: Finding the Right Balance in MedTech” Are Regulations Slowing Innovation?
Navigating the New FDA Quality Management System Regulation: Aligning with ISO 13485 for Global Compliance
Make in India vs Import Dependency: A Reality Check for the MedTech Sector
Regulatory Affairs
Regulatory
Regulatory Strategy
Quality
Quality Assurance
Quality Control
Clinical Post Market Safety / Surveillance
Director
HOD
President
VP
AVP
GM
15+ hours of curated content across 2 days - structured for maximum signal density with zero filler
25+ speakers from regulatory authorities, government bodies, and the C-suites of leading device manufacturers
Exclusive co-location with India Health Exhibition - access to the largest MedTech decision-maker gathering in South Asia.
Formats that drive real engagement: panel debates, fireside chats, one-on-one interview sessions, and structured networking.
Dedicated networking lounge designed to facilitate high-value introductions and partnership conversations.
360° thematic coverage - regulatory strategy, AI & SaMD, quality systems, supply chain resilience, and India manufacturing policy - in one integrated programme.
Direct knowledge access to CDSCO, FDA-aligned, and IMDRF perspectives from officials and practitioners who shape policy.
Regulatory Services
CROs (Contract Research Organization)
Technology
Research Services
Medical Suppliers
PMS Consultants
Consultants
Labelling Consultants
Data Solution Provider
Clinical Services
Quality Regulatory Software / Services
Get in Touch
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