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How to conform with the legal requirements for placing medical devices on the market.
This page provides practical information to help you make the most of your IP when doing business in Kazakhstan.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
How to ensure the products you make or import comply with the law and are safe for consumers to use.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Weights and Measures Act 1985 and subsequent Deregulation Order 1999 (as amended).
If the UKCA marking applies to products you manufacture or supply, you will have specific obligations and responsibilities for compliance, depending on your role.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
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.
Class and permitted use of passenger ships, cargo ships, tankers, tugs, tenders, fishing boats, yachts, commercial vessels, and the required certificates.
Standardisation explained.
Explainer on product information templates to be used by applicants and Marketing Authorisation Holders (MAHs) of veterinary medicines.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines in the UK.
These published standards relate to a number of KPIs in the VMD Deliverables and KPI document.
Guidance on applications and licences for manufacturers & wholesalers, suspended and revoked licences, registrations, exporting medicines, defective medicinal products and fees.
Advice for manufacturers of Class I medical devices for placing products on the UK market
Claim relief on import duty and VAT when importing miscellaneous documents and related articles into the UK.
Requirements for an Animal Test Certificate (ATC) to carry out the field trial of a veterinary medicine in animals (clinical trial) in the UK.
Find out if you will need to use the new UKNI marking and how to use it.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Don’t include personal or financial information like your National Insurance number or credit card details.
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