The European Commission proposed on 23 January more time for companies to apply the In Vitro Diagnostic Medical Devices Regulation (IVDR), under certain conditions, as well as measures to enhance transparency in the medical device sector including speeding up the launch of some elements of the European Database on Medical Devices - EUDAMED.
Klaus Jopp, freelance technical writer for science and technology, previews COMPAMED 2023, including what's on show in Halls 8a and 8b from 13-16 November at Messe Düsseldorf. If you want to see the efficiency of the medical technology industry's supply sector for yourself, a visit to the leading international industry platform COMPAMED in Düsseldorf is essential. More than 700 exhibiting businesses from around 40 different nations will demonstrate their special know-how and many innovations for applications in medical technology, medical devices, and medical technology manufacturing, divided into five "worlds of experience." As always, this will take place in parallel to the thematically fitting world's leading medical trade fair MEDICA with more than 5,000 participants from 70 countries. The five worlds of experience are: manufacturing & devices, services & advice, materials, microtech, as well as IT in Tech. These worlds of experience offer their
IVDR Rollout Brings New Hurdles for Clinical Labs, Smaller Diagnostic Firms in Europe 360dx.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from 360dx.com Daily Mail and Mail on Sunday newspapers.
The UK Government has recently made available a draft of the Medical Devices (Post-market Surveillance Requirements) (Amendment) (Great Britain) Regulations 2023 (2023 Regs). Although.
/PRNewswire/ The "South Korea In-Vitro Diagnostics (IVD) Market (By Technology, Application, Product, End User), Size, Share, Major Deals, Key Players.