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Advice and guidance on the health needs of migrant patients from Colombia for healthcare practitioners.
Information about the EU Regulations and their implementation in Northern Ireland
Covering thalidomide, lenalidomide, and pomalidomide: temporary guidance for pregnancy prevention arrangements for patients taking them during COVID-19
Find out when and how to take samples for testing, and what happens if one of your flocks tests positive.
Order birth, adoption, marriage, civil partnership and death certificates from the General Register Office (GRO) - find GRO index numbers
Guidance to help organisations choose a monitoring approach for stack emissions to air that meets Environment Agency and MCERTS requirements (formerly part of M2).
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.
Look up a trade mark to see if something identical or similar to your brand is already registered.
Information for clinicians and patients.
When tests to detect COVID-19 are commonly used (use cases) and what to consider when deciding which type of test to employ.
Advice and guidance on the health needs of migrant patients from Mexico for healthcare practitioners.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Protocols and procedures for testing the distinctiveness, uniformity and stability (DUS) of certain agricultural and vegetable plants.
Biosecurity and hygiene standards to keep birds safe from bird flu (avian influenza).
How to use A/B testing to evaluate your digital health product.
When and how to take samples for the salmonella national control programme (NCP) if you breed turkeys, and what happens if a flock tests positive.
How the protected online filing (PROOF) scheme can help you prevent fraudulent changes to your company.
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.
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
Guidance on how to prove someone’s identity or give them access to your service or organisation.
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