Everything medical device professionals need to know about promised outcomes of the EU’s MDR, critical issues facing implementation of the EU IVDR, the impact of China’s Order 739 on medical devices, and updated regulations for Thailand now available from the Journal of Medical Device Regulation
The Journal of Medical Device Regulation releases today the contents of its August 2021 issue to non-subscribing readers. The following articles are now publicly available through the Journal’s website – GlobalRegulatoryPress.com:
- Has the European Commission met the needs of manufacturers, healthcare professionals and patients with the MDR and the IVDR?
- Critical issues facing implementation of Regulation (EU) 2017/746 on in vitro diagnostic medical devices with less than a year to application
- What is the impact of China’s new State Council Order 2021/739 on the medical device industry?
- An overview of the new medical device regulations in Thailand
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
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.
