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What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Supports effective delivery of planning application process.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
How to conform with the legal requirements for placing medical devices on the market.
Information about the UK’s points-based immigration system for EU, EEA and Swiss citizens.
The locations for a Marketing Authorisation Holder (MAH) and a Qualified Person responsible for Pharmacovigilance (QPPV)
If the UKCA marking applies to products you manufacture or supply, you will have specific obligations and responsibilities for compliance, depending on your role.
What you need to do to comply with regulations on manufactured goods you place on the EU market.
Find out your VAT obligations if you use an online marketplace to sell goods in the UK.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
Find out if you need to use the UKCA (UK Conformity Assessed) marking on products you manufacture or handle.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Information for businesses on the regulatory framework and transitional arrangements January 2023.
Managing asbestos for your premises, your responsibilities, asbestos regulations, keeping records, health and safety, finding accredited surveyors, penalties
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Pharmacovigilance system requirements
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