Insights on the new Person Responsible for Regulatory Compliance under the European MDR/IVDR, Own Brand Labelling under the MDR, Argentina’s device regulations, and a proposition for Basic Environmental Performance Requirements now available from the Journal of Medical Device Regulation
London, 11 November 2019 – The Journal of Medical Device Regulation releases today the contents of its November 2019 bumper issue of 124 pages 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:
- The new Person Responsible for Regulatory Compliance under the European MDR/IVDR
- MDR: Own brand labelling on life support – can it be saved?
- India’s “New Drugs and Clinical Trials Rules, 2019”: Applicability and impact on medical device clinical investigations
- Basic Environmental Performance Requirements for medical devices: attributes for eco-friendly, green and sustainable medical devices
- An overview of the medical device regulations in Argentina
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 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.
