Interesting read on MDDI about empathy and co-creation in medical device design focusing in users and patients – It’s Time to Meet the Users of…
Posts published in January 2019
Actions that providers and commissioners of health and social care services should take to prepare for, and manage, the risks of a no-deal exit scenario…
Statement from FDA Commissioner Scott Gottlieb, M.D., on the agency’s new actions under the Pre-Cert Pilot Program to promote a more efficient framework for the…
A new report by the US DHS – Health Industry Cybersecurity Practices:Managing Threats and Protecting Patients
Webinar: The role of the TGA in digital health
TGA Consultation: Potential reclassification of active medical devices for diagnosis and patient therapy
TGA Consultation: Changes to a number of definitions and the scope of the medical device regulatory framework in Australia
MHRA response to EU exit no-deal legislative proposals consultation
Further guidance note on the regulation of medicines, medical devices and clinical trials if there’s no Brexit deal