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Information on how to revalidate a UK CoC (and UK GMDSS at the same time).
Check which Authorised Economic Operator status you could apply for and their benefits if your business has role in the international supply chain.
This guide explains key elements of EU law and their history. It accompanies the detailed guide 'Review of the balance of competences'.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
How to qualify as a dangerous goods driver, choosing what training you need, finding a training provider, getting and keeping your ADR card up to date, replacing a card, staying qualified and adding substance classes to your ADR card.
Nomination of BEIS as competent authority for risk-preparedness in the electricity sector.
An overview of the changes made to the Railways (Interoperability) Regulations 2011 that came into force on 1 January 2021.
Information about licence-linked qualifications, the awarding organisations that offer these qualifications, and how to find an approved training provider.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
The Building Safety Regulator's approval criteria for independent schemes that verify the competence of building control professionals and the provider for each scheme.
Apply for an authorisation to manufacture authorised veterinary medicines and medicines marketed under the Exemptions for Small Pet Animals.
Industry must notify the MHRA if they will not be using these flexibilities
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Apply to be an authorised installer for OZEV residential and commercial chargepoint grant schemes.
Guidance for business and government departments.
How to import animals and animal products to Great Britain (England, Scotland and Wales), the Channel Islands and the Isle of Man from non-EU countries.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
This document sets out the minimum competence requirements for organisations and individuals in a competent person scheme.
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