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Register to vote Register by 18 June to vote in the General Election on 4 July.
How we will manage exports if there's a shortage of supply.
Advice for manufacturers of Class I medical devices for placing products on the UK market
List of Field Safety Notices from 20 to 24 May 2024.
Office Supplies Marketplace is an online directory of suppliers for the purchase of office supplies, such as stationery and paper, across the public sector
Certificates you can use when zero rating goods or services under the VAT Act 1994, Schedule 8, Group 15, items 4 to 6.
How veterinary medicines can be advertised.
How to carry out a clinical trial to apply for a marketing authorisation, manage your authorisation and report safety issues.
Information on clinical trials for medicines, how to apply for authorisation in the UK, how to manage your authorisation, reporting safety issues and details about the MHRA phase I accreditation scheme.
A summary of recent letters and notifications sent to healthcare professionals about medicines and medical devices.
Advice on writing clear notices and maximising replies to your FSNs.
Guidance on applications and licences for manufacturers & wholesalers, suspended and revoked licences, registrations, exporting medicines, defective medicinal products and fees.
Guidance on manufacturing, importing, distributing and supplying specially manufactured or ordered products, including cannabis-based products for medicinal use in humans (CBPMs), known as 'specials'
This guidance demonstrates stakeholders, including the government, working together to address supply issues.
How to apply for, update and cancel licences for the manufacture, import and wholesale of human and veterinary medicines.
UK Health Security Agency (UKHSA) culture collections offer a range of products and services for medical science and laboratory healthcare use.
Guidance for healthcare professionals on managing specific medicines and medical devices and using them safely.
How to meet the good clinical practice standards for clinical trials and what to expect from an inspection.
Information on good laboratory, manufacturing and distribution practice, good pharmacovigilance practice (GPvP), out-of-specification investigations, inspection metrics and fees.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
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