Taiwan issues new deadlines for changes and extensions
This article was originally published in Clinica
The Taiwanese Ministry of Health and Welfare has issued a new regulation this month detailing new timelines for applying for regulatory changes for medical devices and drugs.
You may also be interested in...
Those marketing products covered under the EU’s MDR and IVD Regulations have plenty of reading this month to help them prepare. More details have also emerged about the UK’s regulatory future.
Where are the biggest challenges for notified bodies and manufacturers now there is some experience with the MDR, and can the sector manage the new regulatory requirements successfully?
The European Commission has finally published detailed guidance on the EU IVDR’s classification rules. The IVDR’s completely new classification regime means guidance is urgently needed.