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Find out about the changes if you are exporting personal protective equipment (PPE) during the coronavirus pandemic.
Definitive fees charged for applications under Schedule 7 of the Veterinary Medicines Regulations 2013.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Nigeria is subject to regional controls governing small arms and light weapons.
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.
Use an OGEL to export controlled dual-use or military goods, software and technology overseas.
How to apply for an exemption to use a restricted substance to manufacture electrical and electronic equipment.
How to get fast-track approval of medical devices during COVID-19.
Check the tariff classification for the unassembled parts to be implanted into the human body for different spinal treatments.
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
How to use A/B testing to evaluate your digital health product.
You must include the appropriate legal basis for your application when you apply to MHRA for a marketing authorisation.
Goods that are controlled and how to get licences for them, the UK Strategic Export Control Lists, dealing with the Export Control Organisation (ECO).
How to carry out a clinical trial to apply for a marketing authorisation, manage your authorisation and report safety issues.
You must register commercial trailers over 750kg gross weight and all trailers over 3,500kg gross weight before towing them through some European countries.
The Traffic Commissioner for London and the South East's written decision for Hi-Stanford Scaffolding Ltd (OK2042641)
Check the tariff classification for lace-up low shoes.
Check the tariff classification for flavour pods.
Guide to licensing requirements and restrictions for trade control and the export of controlled military goods, software and technology.
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.
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