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How to ensure the products you make or import comply with the law and are safe for consumers to use.
Check the legal requirements you need to meet before you can place a medical device on the market and see how MHRA monitors compliance.
How the Office for Product Safety and Standards contributes to the national regulatory landscape.
VMD Published Standards for regulatory work 2020-2021 against Key performance indicators (KPIs)
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Industry representatives, consumer organisations and other bodies provide advice and expertise on important issues regarding smart meters.
Advice for manufacturers of Class I medical devices for placing products on the UK market
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
VMD Published Standards for regulatory work 2021-2022 against Key performance indicators (KPIs)
How we assess issues of potential regulatory concern
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
What you need to know about and do to comply with the law and keep consumers safe.
An overview of the changes made to the Railways (Interoperability) Regulations 2011 that came into force on 1 January 2021.
Resources for regulators.
The Regulatory Policy Committee provides the government with external, independent scrutiny of the evidence supporting changes in law that affect businesses, charities and community groups.
Guidance for suppliers and dealers.
Tier 2 ecodesign requirements for small, medium and large power transformers are now in force. Use this tool to determine whether the costs of installing Tier 2 transformers are disproportionate.
We set standards for landlords and seek assurance that they are being met.
VMD Published Standards for regulatory work 2022-2023.
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