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Register to vote Register by 18 June to vote in the General Election on 4 July.
Emerging techniques on how to prevent or minimise the environmental impacts of industrial hydrogen production from methane or refinery fuel gas with carbon capture for storage.
Information for British people on medical support in Thailand including mental health, lists of hospitals and care homes and how the British embassy can help.
Find out more about getting authorised consignor or consignee status to start or end transit movements at your own premises.
Guidance for GLP facilities on implementing and maintaining a risk-based quality assurance programme.
How to set up an MOT centre for HGVs, trailers, buses and coaches including eligibility, what you need and how to apply.
We are allowing alternative courses of actions for manufacturing or laboratory equipment during the outbreak.
From 1 October 2024, more materials facilities will need to sample and report their waste. Sampling and reporting will be more detailed and more frequent under the amended regulations.
Access Consortium Statement on Good Manufacturing Practice (GMP) Inspections Reliance and Recognition
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Guidance for those producing, processing, consuming, importing or exporting chemicals covered by the Chemical Weapons Convention (CWC)
Details of funding for multi-sport grassroots facilities projects in 2021 to 2022
Guidance for manufacturers, importers and distributors.
We are producing guidance and information for industry, healthcare professionals and patients covering the coronavirus (COVID-19) outbreak.
Information about when you need to submit substantial amendments to a clinical trial including changes to the trial sponsor or legal representative, Investigational medicinal product certification and importation.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Guidance for organisations involved in any aspect of the pharmaceutical lifecycle or GLP studies regulated by MHRA, covering the approval of paper documents when working from home
Find out how to validate your facility when you seek approval to open, including special requirements for continuous and blood processors.
This guide has been provided to reduce the burden when preparing responses to Post Inspection Letters.
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