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Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
List of Field Safety Notices from 22 to 26 April 2024.
Use these forms if you import, export, or move goods through the UK.
How to apply for an exemption to use a restricted substance to manufacture electrical and electronic equipment.
How investigators and sponsors should manage clinical trials during COVID-19
Marburg virus is a Filovirus which, along with Ebola virus, can cause a severe and often fatal viral haemorrhagic fever (VHF).
Pharmacovigilance system requirements
Make sure that domains that do not send email cannot be used for spoofing.
How to contact MHRA for specific services or enquiries.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Guidance for organisations involved in any aspect of the pharmaceutical lifecycle or GLP studies regulated by MHRA, covering the approval of paper documents when working from home
Look up a trade mark to see if something identical or similar to your brand is already registered.
When tests to detect COVID-19 are commonly used (use cases) and what to consider when deciding which type of test to employ.
Form to report patients meeting the case definition.
How to choose data tools and infrastructure that are flexible, scalable, sustainable and secure.
The requirements for packaging DNLEU
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
Information to help you protect, manage and enforce your intellectual property (IP) rights in China.
Use form C88 (status) as proof of authorisation to import or export for the country of destination.
Use an OGEL to export controlled dual-use or military goods, software and technology overseas.
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