
MHRA Guidance on Portal Registration: Specific Aspects
The new article describes in detail certain specific aspects associated with registrations necessary to make submissions associated with healthcare products.
The new article describes in detail certain specific aspects associated with registrations necessary to make submissions associated with healthcare products.
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.
Overview of China’s National Medical Products Administration (formerly CFDA), their reform, medical device registration, drug registration, …