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This toolkit is for Innovation Passport holders following the Innovative Licensing and Access Pathway (ILAP) and provides activities to support the design and development of medicines.
The New Variant Assessment Platform (NVAP) is an offer of UK capacity and expertise to detect and assess new variants of SARS-CoV-2 around the world.
Information about incidents and outbreaks of Ebola and Marburg, both viral haemorrhagic fevers (VHF).
How to apply for marketing authorisation via this new procedure.
Get authorised to declare goods you bring into Northern Ireland 'not at risk’ of moving to the EU, so that the applicable EU rate of duty will not be payable on those goods.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
How clients can submit and manage a building control application to the Building Safety Regulator for higher-risk building work or building work to an existing higher-risk building.
Find out what areas the Welsh administration legislates on and how it is structured.
This page details the SSRO's latest events
Information for health professionals on the epidemiology, transmission and prevention of Chlamydia abortus which can cause stillbirth or abortion in humans.
The Renewable Transport Fuel Obligation Order regulates renewable fuels used for transport.
How to use a case-control study to evaluate your digital health product.
A collection of documents relating to the government's policy on app security and privacy.
Marking the centenary of the Battle of Amiens and the Subsequent Hundred Days Offensive
How fishing is assessed and managed in marine protected areas (MPA)
The approach the MHRA intends to take for products approved or pending in decentralised procedure (DCP) or mutual recognition procedures (MRP).
Follow this guidance to submit information to the Cabinet Office on all consultancy and professional services spend at or above the thresholds specified below.
How UK private maritime security companies (PMSCs) get sealed and signed physical certificates to meet documentation requirements of overseas governments.
Definitive fees charged for applications under Schedule 7 of the Veterinary Medicines Regulations 2013.
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