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Economic and consumer standards that registered providers of social housing must comply with.
There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
Information about the EU Regulations and their implementation in Northern Ireland
Withdrawn – Not deemed regulatory material.
Find out about Ofqual's rules for the qualifications and assessments we regulate.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Standardisation explained.
Information on the UK government’s framework to create UK Sustainability Disclosure Standards (UK SDS) by assessing and endorsing the global corporate reporting baseline of IFRS Sustainability Disclosure Standards.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
Lists of standards that businesses can use to show their products, services or processes comply with essential requirements of legislation.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
What you need to know about and do to comply with the law and keep consumers safe.
This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications
Published standards for regulatory work 2023/24
What is involved in regulatory judgements and gradings
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
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