The medical device industry in India is a rapidly growing sector, propelled by increasing healthcare needs, technological advancements, and supportive initiatives such as the PLI Scheme and Make in India. India offers immense opportunities for innovation in medical devices, making it vital to promote domestic manufacturing and evolve regulatory and quality strategies to support the sector’s growth.
On these lines, the 8th Annual Medical Device Regulatory and Quality Summit 2024 took place on August 22-23, 2024, in Aerocity, New Delhi, bringing together experts and stakeholders from across the medical device industry. The summit provided a comprehensive platform to discuss the latest developments, regulatory updates, and quality management practices shaping the future of medical devices globally. The event featured insightful panel discussions on critical topics such as the regulations governing medical devices in India, emerging cybersecurity trends, risk management aligned with ISO standards, and global medical device classification. Other sessions included registration requirements across India, the USA, the EU, Australia, Russia, China, and Brazil, patient safety, clinical evaluation, and MDR certification strategies.
Preeti Tyagi and Akash Dixit from LexOrbis participated in the summit, gaining valuable insights into the evolving regulatory and quality frameworks and representing LexOrbis’s dedication to supporting the growth and innovation of the medical device industry.