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The MHRA is ready to provide any assistance for clinical trials applications submitted for COVID-19
You must tell DVLA if you have a brain abscess, cyst or encephalitis - download the correct form to let them know
The epidemiology, symptoms, diagnosis and management of Nipah virus infections.
Covering thalidomide, lenalidomide, and pomalidomide: temporary guidance for pregnancy prevention arrangements for patients taking them during COVID-19
Listing of countries with a known occurrence of high consequence infectious disease (HCID).
Use this form to file a translation in connection with a European patent or a European patent application
Find out which birds and animals may be spared from culling during an outbreak of an exotic animal disease.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Form to report patients meeting the case definition.
When tests to detect COVID-19 are commonly used (use cases) and what to consider when deciding which type of test to employ.
Guidance to help organisations choose a monitoring approach for stack emissions to air that meets Environment Agency and MCERTS requirements (formerly part of M2).
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.
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.
Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
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.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
Information on carrying medicine containing controlled drugs for individual travellers entering or leaving the UK.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
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