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Pharmacovigilance system requirements
This document explains: how patients are tested and treated, and steps in place to prevent its spread.
Actions that trial sponsors should consider to build resilience into clinical trial design
How to apply for an exemption to use a restricted substance to manufacture electrical and electronic equipment.
When tests to detect COVID-19 are commonly used (use cases) and what to consider when deciding which type of test to employ.
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.
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
Use a separate statement of objection form for each Japanese GI product name you object to.
Information and advice on rabies, the viral infection of the central nervous system which affects mammals and humans.
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.
Volume 19 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
How to spot Batrachochytrium salamandrivorans, what to do if you suspect it and measures to prevent its spread.
How to contact MHRA for specific services or enquiries.
Applications received to amend the specification of a patent under sections 27 and 75 before the court and the Office.
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.
Paper and cardboard production can cause significant pollution. This guide describes industry responsibilities for preventing pollution.
Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
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