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Get information on teacher training courses, funding, pay scales and how to make a great application
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Marburg virus is a Filovirus which, along with Ebola virus, can cause a severe and often fatal viral haemorrhagic fever (VHF).
Pharmacovigilance system requirements
Advice and guidance on the health needs of migrant patients from Colombia for healthcare practitioners.
This document explains: how patients are tested and treated, and steps in place to prevent its spread.
Information about the EU Regulations and their implementation in Northern Ireland
Listing of countries with a known occurrence of high consequence infectious disease (HCID).
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Find out which birds and animals may be spared from culling during an outbreak of an exotic animal disease.
Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
Information for clinicians and patients.
Look up a trade mark to see if something identical or similar to your brand is already registered.
Information for British citizens moving to or living in Colombia, including guidance on residency, passports, healthcare and emergencies.
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
Apply for a Temporary Work - Religious Worker visa to do religious work in the UK - getting sponsored, fees, eligibility, family members
You must include the appropriate legal basis for your application when you apply to MHRA for a marketing authorisation.
How to use A/B testing to evaluate your digital health product.
How to carry out a clinical trial to apply for a marketing authorisation, manage your authorisation and report safety issues.
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