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Standardisation explained.
Ofqual's formal legal list of Regulatory Documents (documents containing additional rules and guidance for regulated qualifications).
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
RA withdrawn, contents incorporated into another document as detailed within.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
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
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
How to ensure the products you make or import comply with the law and are safe for consumers to use.
This guidance provides an introductory guide to the standards and regulatory requirements that businesses may need to meet, to import and sell goods in the UK.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
The requirements that registered providers of social housing must meet.
Guidance for manufacturers, importers and distributors.
Information about RSH's regulatory standards, how we regulate registered providers, our information requirements and other guidance
RA Withdrawn – Content duplicated in RA 5203.
Lists of standards that businesses can use to show their products, services or processes comply with essential requirements of legislation.
Withdrawn – Not deemed regulatory material.
Find out about Ofqual's rules for the qualifications and assessments we regulate.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
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