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Register to vote Register by 18 June to vote in the General Election on 4 July.
Submission dates and how the submissions using the EC decision reliance procedure work.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
5 quick tips on submitiing your paper for review
Submissions related to human medicines need to be submitted directly to the MHRA.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
Use this form to submit an article to feature in a future edition of the serious and organised crime (SOC) local partnerships bulletin.
Guidance on the submission, processing and assessment of all completed paediatric studies sponsored by Marketing Authorisation Holders (MAHs)
Marketing Authorisation Holders should review their manufacturing processes to identify and, if found, to mitigate the risk of nitrosamine impurities being present.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
How to submit an application, data package and responses for proposed or existing marketing authorisations.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
You should follow the standard file process outlined below when submitting work for online and paper billing.
Instructions on how members of the public can submit their submissions to support the work of the team of experts leading the review.
The Marine Management Organisation (MMO) is preparing to help our fishing and seafood industries to be ready to trade successfully in the international marketplace from 1st January 2021.
The New Active Substance Work Sharing Initiative (NASWSI) has successfully approved several medicines through this international collaboration and continues to foster cooperation and strong relationships between its Access partners. The Biosimilar Work Sharing Initiative (BSWSI) builds on this success.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Pharmacovigilance system requirements
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Submission of notifications for northern Ireland under article 20 of directive 2014/40/EU.
Don’t include personal or financial information like your National Insurance number or credit card details.
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