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. Key topics include risk management integration, preclinical and clinical planning, and post-market surveillance. Discussions will focus on common regulatory challenges, MDSAP insights, and navigating AI-based device regulations. The conference aims to equip participants with strategic insights and tools for successful market entry and improved patient care. This conference is essential for MedTech professionals to deepen their understanding of QA and RA, ensuring regulatory compliance and fostering innovation.
This conference is crucial for professionals in medical technology, medical device manufacturing, medical equipment manufacturing, medical supplies, healthcare technology, healthcare solutions, medical electronics, and biomedical devices. It aims to equip participants with strategic insights and tools for successful market entry and improved patient care. MedTech professionals will benefit from in-depth discussions on QA and RA, ensuring regulatory compliance and fostering innovation in their fields.
