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How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
Clarification for the interpretation of the new elements within the Veterinary Medicines Regulations (VMRs), as amended, relating to combating antimicrobial resistance (AMR).
Follow this guidance to request spend approval when buying or extending facilities management contracts, regardless of their cost.
Information on trade sanctions, arms embargoes and trade restrictions, including trade controls, transit controls and restrictions on terrorist organisations.
Guiding principles for the use of predetermined change control plans (PCCPs) for managing rapid product changes in medical devices.
Development of a standard approach for AI and autonomy in networked multi-sensor systems in security and defence.
A summary of the main methods you should use to analyse ambient air monitoring data.
Find out which radioactive sources you need a licence to export and how to apply for one.
Information on reversions for members of the public.
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