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Register to vote Register by 18 June to vote in the General Election on 4 July.
AMRHAI (antimicrobial resistance and healthcare associated infections) is the national reference unit for investigating AMR in healthcare-associated bacteria.
The Medicines and Healthcare products Regulatory Agency (MHRA) has today (9 May 2024) launched AI Airlock, its new regulatory sandbox for AI as a Medical Device (AIaMD).
Information for patients, public and health care professionals.
A proactive, collaborative, agile and the first of its kind approach to identifying and addressing the challenges faced by AI as a Medical Device (AIaMD).
The way you apply to licence biological products has changed
The Military Aviation Authority is responsible for the regulation, assurance and enforcement of the defence air operating and technical domains. MAA is part of the Ministry of Defence and the Defence Safety Authority .
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
The Advisory Group on Military and Emergency Response Medicine (AGMERM) provides specialist advice to the Ministry of Defence on the medical aspects of defence against chemical, biological and radiological threats. AGMERM works with the Ministry of Defence .
The MHRA is continuing to accept Active Substance Master Files (ASMFs) and Certificates of Suitability (CEPs)
How an innovative funding mechanism is saving lives by speeding up the availability of vaccines and making them affordable.
Information about MAA ATM equipment certification, which ensures ATM equipment designs meet appropriate safety requirements.
Apply for a promising innovative medicine (PIM) designation or scientific opinion for your medicine from MHRA.
The ASMAT can provide an assessment of the current performance of the air safety management system (ASMS) and show any further development needed.
A review of MDMA (‘ecstasy’), its harms and classification under the Misuse of Drugs Act 1971 (2009). The Advisory Council on the Misuse of…
Guidance to help organisations choose a monitoring approach for stack emissions to air that meets Environment Agency and MCERTS requirements (formerly part of M2).
We help people, businesses and the UK economy by promoting competitive markets and tackling unfair behaviour. CMA is a non-ministerial department.
How to get a marketing authorisation for an Advanced Therapy Medicinal Product (ATMP) so it can be sold and/or supplied in Great Britain.
Apply for an authorisation to manufacture extemporaneous preparations, autogenous vaccines, stem cell products or blood products for non-food animals.
Information about MAA certification which ensures that an air system's design meets appropriate safety requirements.
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