15th - 16th October 2024
Le Méridien, New Delhi
15th - 16th October 2024
Le Méridien, New Delhi
The Indian medical devices market is currently estimated at $11 billion and is expected to grow to $50 billion by 2025, with the sector experiencing a steady growth rate of 15% CAGR over the last three years. This remarkable growth is driven by continuous innovation in medical technology, responding to evolving patient needs and technological advancements.
The medical device industry has seen significant innovation over the past decade, driven by patient needs and technological progress. Navigating device development and regulatory approval demands expertise in quality assurance (QA) and regulatory affairs (RA). Experts will discuss regulatory compliance, technological specifications, and evolving patient demands from concept to market launch. Speakers from QA and RA fields will share practical methods for regulatory strategy strengthening, compliance with standards, and navigating global requirements.
Panel Discussion & Fire Side Chats
8+
Partners
25+
Industry Leaders
15+
Networking sessions
Notified Body perspective: Progress made& status of MDR & IVDR .
Indian MedTech: Discussing regulatory & policy framework.
The impact of 2017 MDR & IVDR on SMEs.
How to effectively develop pre-market clinical trials.
Medical device safety: Finding the right balance between proactive post market safety and vigilance.
Digital health: Evaluating current trends, opportunities and challenges.
Extended MDR & IVDR deadline – How can manufacturers leverage the extended deadline.
Explore how digital innovations are reshaping the MedTech landscape.
Engage in discussions on India's regulatory and policy framework for the MedTech industry and understand its implications for your business.
Learn how 2017 MDR and IVDR impact SMEs and strategies to overcome challenges.
Learn best practices to uphold excellence in manufacturing and ensure your devices meet the highest standards.
Understand how to create and maintain a robust quality management system that adapts to industry challenges and ensures product reliability.
Effectively developing and managing pre-market clinical trials for regulatory compliance and market readiness.
Get updates from notified bodies on MDR and IVDR advancements.
Explore how to use cybersecurity as a tool for business growth.
Stay ahead with the latest in digital labelling technologies, improving compliance and enhancing product information management.
Manging Director & Forum Coordinator (AiMeD)
Director-Health Economics & Govt Affairs
Team Leader of reviewers of "drugs"
Senior Vice President – Regulatory Affairs & Quality Assurance
Vice President
Advisor- Public Health Administration NHSRC-MoHFW GOI
Chief Executive Officer
Chief Operating Officer"
Partner & National Lifesciences Leader"
Head - Medical & Health Services, South Asia
Sr. Vice President
Managing Director India & South Asia
Lead Auditor of ISO 13485:2016 / Medical Device Officer for CDSCO Licensing
Associate Director, Quality India/South Asia
Director-Quality Assurance and Regulatory Affairs- JAPAC
Director - Regulatory Affairs
Senior Director, Quality and Regulatory Affairs, Asia Pacific
Associate Director
Director Regulatory Affairs and Quality Assurance
Lead System Designer
Senior Manager – Cyber Security
Head: Regulatory Affairs, Greater India
Director - APAC (DSO & Commercial Strategy)
One of its kind of platforms with key focus on MedTech from a 360-degree approach.
The conference is spread across distinct verticals and themes covering various aspects of MedTech.
An opportunity to connect with more than 150+ industry professionals.
Top speakers from the industry majorly the Directors, Presidents, VPs of top medical device & diagnostic companies, regulatory authorities and government bodies.
Visibility of vendor’s product with primary industry decision-makers.
Increased brand awareness and visibility.
