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How to write requirements for services on the Digital Outcomes and Specialists framework
Find out how to prove the originating status of your goods and check if you can claim preferential tariff treatment.
Submissions related to human medicines need to be submitted directly to the MHRA.
This paper outlines the methodology used for the 2012 GHG Conversion Factors. These have been superseded by the 2013 factors, integrated into a web based tool.
Guide to the submission process.
How the MHRA processes variations to Marketing Authorisations (MAs)
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
The process for applicants applying for a Paediatric Investigation Plan (PIP) modification or waiver.
Guide to the data submission process.
Check what you need to do if you're sending, receiving and storing VAT invoices in an electronic format.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Information for British citizens moving to or living in the Netherlands, including guidance on residency, healthcare and driving.
Information for British citizens moving to or living in Austria, including guidance on residency, healthcare and driving.
Provides further information in support of the implementation of waste planning policy.
The report provides some initial notes for guidance, an annotated briefing paper structure and 2 worked examples
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
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