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Register to vote Register by 18 June to vote in the General Election on 4 July.
Explanation of legal phrases used in the Civil Procedure Rules.
Explanation of legal phrases used in the Family Procedure Rules.
Submission dates and how the submissions using the EC decision reliance procedure work.
Guidance explaining why compulsory purchase orders are made, and what people's rights are to challenge them.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Technical advice and guidance for licence holders.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Extradition processes and agreements between the UK and other countries, role of the Secretary of State, High Court and Supreme Court.
Helping public health practitioners conducting evaluations – using process evaluations to explain how complex interventions work.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
How to apply for marketing authorisation via this new procedure.
How to run exercises and training for emergency planning and preparedness, with an introduction to the Central Government Emergency Response Training (CGERT) Course.
Upper Tribunal Administrative Appeals Chamber decision by Judge Brunner on 3 May 2024.
Guidance on the fast-track process for Nationally Significant Infrastructure Projects.
This service allows hospitals to record incidents of infection after surgery, track patient results and review or change practice to avoid further infections.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
The latest versions of the Criminal Procedure Rules and of the Criminal Practice Directions made by the Lord Chief Justice.
Statutory Instruments that relate to the Criminal Procedure Rules.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
The approach the MHRA intends to take for products approved or pending in decentralised procedure (DCP) or mutual recognition procedures (MRP).
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