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Data, Freedom of Information releases and corporate reports
Information about the EU Regulations and their implementation in Northern Ireland
Actions that trial sponsors should consider to build resilience into clinical trial design
Listing of countries with a known occurrence of high consequence infectious disease (HCID).
AVU provides services for genotypic antiviral resistance testing of HIV and HCV, investigation of HIV transmission events and HSV antiviral resistance testing by phenotyping.
Covering thalidomide, lenalidomide, and pomalidomide: temporary guidance for pregnancy prevention arrangements for patients taking them during COVID-19
Guidance to help organisations choose a monitoring approach for stack emissions to air that meets Environment Agency and MCERTS requirements (formerly part of M2).
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Find out which birds and animals may be spared from culling during an outbreak of an exotic animal disease.
Look up a trade mark to see if something identical or similar to your brand is already registered.
The UK Good Laboratory Practice Monitoring Authority (UK GLPMA) recognises that there are potential challenges COVID-19 will present to members of the GLP monitoring programme.
Find out who can get a free rapid lateral flow test, how to use the test and what your test result means.
How to use A/B testing to evaluate your digital health product.
How to do a Getein Biotech rapid nose-only test for COVID-19. Rapid tests show the result on a device that comes with the test.
Use form C88 (status) as proof of authorisation to import or export for the country of destination.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
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
Information to help you protect, manage and enforce your intellectual property (IP) rights in China.
Licences and authorisations to import genetic material, research and diagnostic samples, trade samples and display items, and some live animals and animal products.
Monitor the progress of a patent application through search reports, open to the public inspection files, and caveats.
You must include the appropriate legal basis for your application when you apply to MHRA for a marketing authorisation.
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