The impact of the new EU Market Surveillance Regulation, China’s regulatory reforms in 2020, Advertising under the European MDR/IVDR, Classification of borderline devices, Egypt’s device regulations, and an Analysis of the new US guidance on nitinol-containing medical devices now available from the Journal of Medical Device Regulation
London, 10 February 2020 – The Journal of Medical Device Regulation releases today the contents of its February 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:
- Is there still a problem with the classification of certain borderline medical devices in Europe?
- The impact of the new Market Surveillance Regulation on MDR- and IVDR-regulated medical devices and IVDs
- Advertising medical devices in the EU – Do the MDR and IVDR represent a change in EU law?
- As China’s regulatory reforms continue apace, what can we expect in 2020?
- An analysis of the US FDA’s draft guidance on nitinol-containing medical devices, and the reasons for its development
- An overview of the medical device regulations in Egypt
About the Journal of Medical Device Regulation
The Journal of Medical Device Regulation 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 further information
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.
