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Register to vote Register by 18 June to vote in the General Election on 4 July.
Information about the EU Regulations and their implementation in Northern Ireland
This white paper covers government’s aims to ensure the UK regulatory landscape delivers a world class service.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
This collection includes short guidance notes on specific appraisal or better regulation framework subjects. They complement the RPC's main guidance documents.
How RSH uses, and intends to use, its statutory regulatory and enforcement powers and certain general powers (from 1 April 2024)
Plans showing how departments and their regulators are ensuring that their approach to regulation supports innovation.
The Office of Rail Regulation (ORR) is the independent safety and economic regulator for Britain’s railways. It is responsible for ensuring that railway operators comply with health and safety law. It regulates Network Rail’s activities and funding requirements, regulates access...
Guidance to government departments on the RPC's scrutiny process.
The Medicines and Healthcare products Regulatory Agency regulates medicines, medical devices and blood components for transfusion in the UK. MHRA is an executive agency, sponsored by the Department of Health and Social Care .
Practical ways councils can make good use of their regulatory services.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Find out about Ofqual's rules for the qualifications and assessments we regulate.
Alerts and warnings issued by the commission about particular risks or vulnerabilities which could affect charities and their operations.
Following MHRA approval of a clinical trial, a study on Nuwiq, a recombinant FVIII therapy for the treatment of haemophilia A, can proceed.
The Regulators' Compliance Code is designed to embed a risk-based, targeted approach to regulatory inspection and enforcement.
There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
Check the legal requirements you need to meet before you can place a medical device on the market and see how MHRA monitors compliance.
A speech delivered by the Chair of the Competition and Markets Authority, Marcus Bokkerink.
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