Just released: Important information for European Class I medical device manufacturers, a summary of current Post-Market Clinical Follow-Up requirements, Vietnam’s device regulations, and more essential articles now available from the Journal of Medical Device Regulation
The Journal of Medical Device Regulation releases today the contents of its August 2019 issue to non-subscribing readers.
The August 2019 issue of the Journal of Medical Device Regulation is out now and provides medical device professionals with useful information and reference for their day-to-day business. The following articles are now publicly available through the Journal’s recently relaunched website – www.GlobalRegulatoryPress.com – 10 days after their official publication in the Journal:
- Post-Market Clinical Follow-up (PMCF) requirements under the EU Medical Device Regulation (MDR)
- Class I manufacturers – are you ready for the MDR deadline?
- An overview of the medical device regulatory requirements in Vietnam
- The revision of ISO 14155
- Resolving issues prior to submission of a US FDA 510(k) application
Customers interested in the whole issue may purchase it through the Journal‘s website too.
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, electronic publication.
For further information
For more information on the Journal of Medical Device Regulation, please contact Marija Capek (tel: +44 7916 443811), email: sales@globalregulatorypress.com) or visit www.GlobalRegulatoryPress.com.
