The global medical devices market size was valued at $425.5 billion in 2018 and is expected to reach $612.7 billion by 2025, grow at a CAGR of 5.4%. More than 180,000 U.S. companies are involved in designing, developing, manufacturing, testing, marketing, packaging, and distributing medical devices in this thriving market. Today's Medical Developments serves the need of manufacturers and design professionals in medtech by featuring products, services, and techniques to help improve design and manufacture processes.
How to Manage Massive Medical Device Packaging Changes Abhishek Gautam, director of global packaging for medical device manufacturer Teleflex, shares tips on how to stay ahead of risks while addressing your legacy packaging designs and testing to comply with the European Union Medical Device Regulation (EU MDR).
When a regulatory change requires you to revisit your legacy product testing or update virtually all your package designs, the massive workload could be daunting, especially for small or busy packaging departments. But the situation also gives you the unique opportunity to reimagine your packaging for cost reduction, production performance, and perhaps most importantly user experience and safety.
ComplianceOnline Hosts Seminar on MDSAP Implementation & Participating Country Regulatory Processes: U S, Canada, Brazil einnews.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from einnews.com Daily Mail and Mail on Sunday newspapers.
Note From the Editors
The pace of impact through digital health in 2021 is off to a rapid start be it the number of transactions, the numerous legislative proposals and actions, or the focused attention of enforcement bodies. Given the accelerated pace of tech-enabled methods, such as telehealth or product development through streamlined digital tools and decentralized clinical trials, not to mention AI and big data s impact on diagnostic and research capacity, the policy and regulatory spotlight on digital health will no doubt be bright throughout this year. In the Industry Insights contribution for this issue, several of our digital health experts briefly summarize the focused attention of U.S. enforcement agencies on telehealth given significantly increased reimbursement trends in the area.
Note From the Editors
The pace of impact through digital health in 2021 is off to a
rapid start be it the number of transactions, the numerous
legislative proposals and actions, or the focused attention of
enforcement bodies. Given the accelerated pace of tech-enabled
methods, such as telehealth or product development through
streamlined digital tools and decentralized clinical trials, not to
mention AI and big data s impact on diagnostic and research
capacity, the policy and regulatory spotlight on digital health
will no doubt be bright throughout this year. In the Industry
Insights contribution for this issue, several of our digital
health experts briefly summarize the focused attention of U.S.