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Sep 12, 2020
Sep 7, 2020
MHRA Submission: The Role of Initial Company Administrator
The UK has
left the EU, and the transition period after Brexit comes to an end this year. From
1 January 2021, for medicines authorized in Great Britain, Marketing Authorization
Holder (MAH), will be required to submit pharmacovigilance...
Sep 4, 2020
How to gain access for performing submissions to the MHRA from 1 January 2021
The following
groups will need to take access to MHRA Submissions in order to start submissions
from 1 January 2021:
All
pharmaceutical companies involved in making medicines regulatory submissions
and vigilance activitiesAll
medicines...