Great Britain
The new article describes in detail certain specific aspects associated with registrations necessary to make submissions associated with healthcare products.
Great Britain
The article highlights the key points related to the registration process to be completed by interested parties to be able to make submissions via the e-submission system implemented in the UK.
India
Experts and pharmaceutical companies in India may grant terminally ill patients access to drugs that have not yet been cleared through clinical trials. The new policy would serve as a last resort for patients who are left with no available approved treatments. A draft...
China
What is the NMPA The China Food and Drug Administration (CFDA), or the now National Medical Products Administration (NMPA), is the Chinese regulating body that oversees pharmaceuticals, medical devices, and cosmetics. Some of their tasks and responsibilities include:...
EU MDR/IVDR
On Friday, the European Medicines Agency (EMA) released two guidance documents addressing issues surrounding drug shortages in the EU, and how to manage drug shortages publicly. These documents were created by a task force specifically to aid in companies’ reporting...
