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Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
Volume 20 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
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 get fast-track approval of medical devices during COVID-19.
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.
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 apply for an exemption to use a restricted substance to manufacture electrical and electronic equipment.
Examples of how and when to adjust the customs value for commercial level and quantity when using Methods 2 or 3 if you’re an importer or clearing agent.
The Traffic Commissioner for London and the South East's written decision for Hi-Stanford Scaffolding Ltd (OK2042641)
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.
Guide to licensing requirements and restrictions for trade control and the export of controlled military goods, software and technology.
Volume 31 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Use this form to transform your Madrid Protocol Designation to a UK Trade Mark application.
These temporary good manufacturing practice (GMP) flexibilities will be allowed to address the current exceptional circumstances
Get help to classify drones and aircraft parts for import and export.
Volume 43 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Legal terms for veterinary medicines, marketing of non-medicinal products including medicinal words and phrases, how to complain.
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