The medical device industry makes an enormous number of products—ranging from surgical gloves to artificial joints and imaging equipment. It plays a crucial role in developing new medical technologies that can improve the ability to diagnose and treat illness. But do you know the industry trends that will influence the introduction of new products in 2019? Or what impact they will have on compliance, or how the new technology will shape the year?
Get the answers to all these questions (and more) in this webinar by industry expert Milind Nadgouda. Nadgouda will provide expert insight on the medical device industry’s achievements in 2018, and what to expect in 2019—starting with a background on medical devices trends over the past 3 years, as well as supporting global legislations, with specific emphasis on certain types of devices. Nadgouda will walk you through the five key things to expect in 2019, explain why they are important, and what impact they will likely have on the industry. You will learn about the potential challenges to expect on a global level, as well as the opportunities that could exist within the industry with emerging technologies, the constraints in the existing ones, and the likely threats perceived by the industry.
This session will bring you up to speed with:
Who Should Attend
Ask a question at the Q&A session following the live event and get advice unique to your situation, directly from our expert speaker.
Milind Nadgouda is a seasoned quality and regulatory professional with 19 years of industry experience. He is the co-founder and director at RiverArk Limited, a quality consultancy providing services in the GxP space. His core areas of specialisation are risk strategy (identification, assessment, rating, prevention, and mitigation); regulatory agency inspection readiness, and quality management system GAP analysis.