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Routine resurveys are undertaken in areas where the seabed itself is highly mobile.
How to confirm a measles diagnosis, manage cases and contacts, control infection, and vaccinate young or partially-covered patients.
News and guidance on veterinary medicines issues affected by coronavirus (COVID-19).
Guidance primarily aimed at local responders covering some humanitarian issues that may arise during the recovery phase of an emergency in the UK.
Find out when and how to take samples for testing, and what happens if one of your flocks tests positive.
Guidance for the veterinary pharmaceutical industry on the production and submission of the Summary of Product Characteristics (SPCs) and product literature mock-ups.
We work for a secure and prosperous United Kingdom with global reach and influence. We will protect our people, territories, values and interests at home and overseas, through strong armed forces and in partnership with allies, to ensure our security,...
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.
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
Find out about the symptoms of COVID-19, what to do if you or your child has them and when to get medical help.
How to use a combination of quantitative and qualitative data to evaluate your digital health product.
Find out when and how to take samples, and what happens if one of your flocks tests positive.
Advises on how to consider light within the planning system.
Information about COVID-19 and pregnancy from the Royal College of Obstretricians and Gynaecologists (RCOG).
Information on the potential health impacts of drought in England and the measures that people can take to stay healthy during these events.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
These temporary good manufacturing practice (GMP) flexibilities will be allowed to address the current exceptional circumstances
Guidance for industry on flexible approaches we are taking on good distribution practices.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
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