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Type approval, individual (IVA), motorcycle single vehicle approval, voluntary approval, certificate of initial fitness, accessibility approval, fees, forms, replacement certificates
The MHRA has approved the combined antibiotic cefepime/enmetazobactam (Exblifep 2 g/0.5 g powder for concentrate for solution for infusion)
Information to support commercial fishers on under 12 metre English vessels.
Information for healthcare professionals and the public on Moderna's bivalent vaccines. Information on the original Spikevax COVID-19 vaccine can found on a separate page (link below)
Find out how to propose your own (method 7) method for processing animal by-products (ABPs) instead of using one of the 6 standard methods.
How to set up and run a motorcycle approved training body (ATB) to provide compulsory basic training (CBT) and the direct access scheme (DAS) to learner riders
How to get a licence (grant of approval) to hold a civil marriage or civil partnership in your venue, and what requirements or conditions to follow
The Medicines and Healthcare products Regulatory Agency (MHRA) has today (9 April 2024) approved the medicine fosdenopterin (Nulibry) to treat the genetic disease Molybdenum Cofactor Deficiency (MoCD) Type A
Apply to be a waste electrical and electronic equipment (WEEE) producer compliance scheme and operate legally under your approval.
High-level overview of the approval process and the role of each organisation in the process.
This marine information note (MIN) has been published to advise of a recent decision made regarding the acceptance of electronic record books under MARPOL as listed in resolution MEPC.312(74).
Information for healthcare professionals and the public about the adapted Spikevax XBB.1.5 vaccine
The CMA has accepted commitments offered by Google that address the CMA’s competition concerns resulting from investigating Google’s proposals to remove third-party cookies and other functionalities from its Chrome browser.
UK approved bodies listed under Medical Devices Regulations 2002 (SI 2002 No 618, as amended) (UK MDR 2002).
How the moratorium affects our funded qualification offers and information about exemptions.
An Internal review undertaken following a request about the AMI authorisation process.
Launched in January 2024, IRP aims to further help bring life-saving new medicines to UK patients without delay
How test manufacturers or distributors can apply for approval of their tests to sell on the UK market.
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