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Information about the EU Regulations and their implementation in Northern Ireland
Advice and guidance on the health needs of migrant patients from Argentina for healthcare practitioners.
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
This toolkit is for Innovation Passport holders following the Innovative Licensing and Access Pathway (ILAP) and provides activities to support the design and development of medicines.
When tests to detect COVID-19 are commonly used (use cases) and what to consider when deciding which type of test to employ.
How to spot contagious epididymitis, what to do if you suspect it and measures to prevent its spread.
The family procedure rules are a single set of rules governing the practice and procedure in family proceedings in the high court, county courts and magistrates' courts.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Look up a trade mark to see if something identical or similar to your brand is already registered.
The requirements for packaging DNLEU
Find out how to do a rapid lateral flow test for COVID-19. Rapid lateral flow 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
Volume 52 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Use form C88 (status) as proof of authorisation to import or export for the country of destination.
Volume 20 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Find out who can get a free rapid lateral flow test, how to use the test and what your test result means.
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.
Monitor the progress of a patent application through search reports, open to the public inspection files, and caveats.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
Form to report patients meeting the case definition.
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