Essentials for medical device regulatory professionals now available from the Journal of Medical Device Regulation: regulatory development in Eurasia, guidance on the use of RWE, MD regulations in Vietnam, and obtaining CFSs in Europe
The Journal of Medical Device Regulation releases today the contents of its February 2022 issue to non-subscribing readers.
The following articles are now publicly available through the Journal’s website – GlobalRegulatoryPress.com:
- An overview of the new Eurasian medical device regulatory environment from 1 January 2022
- Real-world evidence for medical device evaluation: Guidance and approaches to support regulatory decision-making in the USA
- An overview of the medical device regulations in VietNam
- Obtaining a Certificate of Free Sale (CFS) in Europe: Part 2
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.
