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Get endorsement for the Global Talent visa to work in the UK as a researcher or academic leader - fellowship, UKRI endorsement, peer review.
Check the regulations on aircraft parts imported with a certificate of airworthiness.
Find out about the changes if you are exporting personal protective equipment (PPE) during the coronavirus pandemic.
Check the tariff classification for four-wheeled vehicles powered by an electric motor fitted with a hydraulic lifting device and telescopic jib.
Apply for a Secondment Worker visa to work for a UK organisation as part of a high-value contract - eligibility, fees, documents, extend, switch or update, bring your partner and children.
Apply for an Academic Technology Approval Scheme (ATAS) certificate, to study certain subjects in the UK.
Helping public health practitioners conducting evaluations on how to plan them.
Definitive fees charged for applications under Schedule 7 of the Veterinary Medicines Regulations 2013.
How to legally run a business that deals with the wholesale of animal medicines (veterinary medicinal products) and the WDA Register.
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
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.
UK Health Security Agency's laboratories provide a comprehensive range of microbiological tests and services.
How to apply for an exemption to use a restricted substance to manufacture electrical and electronic equipment.
Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
What you need to do to work and operate in the aviation industry.
Use an OGEL to export controlled dual-use or military goods, software and technology overseas.
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.
How to get fast-track approval of medical devices during COVID-19.
List of hospitals and medical facilities for British nationals in France
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.
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