Everything manufacturers need to know about the new EU IVDR, requirements for new interactions with Notified Bodies for combination products, promotion of devices in the USA through new media, medical reversals and retractions in clinical evaluations, and updated rules for Argentina now available from the Journal of Medical Device Regulation
London, 10 May 2020 – The Journal of Medical Device Regulation releases today the contents of its May 2020 issue to non-subscribing readers.
The following articles are now publicly available through the Journal’s website – GlobalRegulatoryPress.com – 10 days after their official publication in the Journal:
- What do in vitro diagnostic (IVD) manufacturers need to know about the new EU IVD Regulation?
- An overview of US regulations and policies regarding promotion of medical devices through websites and social media
- A Notified Body’s perspective on the requirements for new interactions with Notified Bodies under the MDR with respect to combination products
- Medical reversals and retractions in clinical evaluations
- An updated overview of the medical device regulations in Argentina
About the Journal of Medical Device Regulation
The Journal of Medical Device Regulation (founded in 2004) reaches regulatory professionals around the world and provides them with in-depth articles on current regulatory matters as well as topical information on international regulatory changes. In addition to publishing review and discussion articles by opinion leaders from the device community, the Journal summarises the global news headlines and provides useful reference information in the form of charts and briefing documents. The Journal is a quarterly, subscription-only publication that is available in electronic format.
For more information on the Journal of Medical Device Regulation, please contact us (tel: +44 7916 443811), email: sales@globalregulatorypress.com) or visit GlobalRegulatoryPress.com.
