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Criteria that all qualifications need to meet to be approved for funding.
Renewal application form for verified gross mass of containers
The Medicines and Healthcare products Regulatory Agency (MHRA) has today (30 January 2024) approved the medicine momelotinib (Omjjara) to treat the symptoms experienced by adult myelofibrosis patients who have moderate or severe anaemia (a low number of red blood cells...
Information on how to apply for approval to use raw tobacco in a controlled activity.
The Marine Management Organisation (MMO) is conducting a programme to assess vessel monitoring systems to identify devices that meet its technical specifications for reporting of location, heading and speed by under 12m fishing vessels.
The Medicines and Healthcare products Regulatory Agency (MHRA) has designated two new UK Approved Bodies, delivering increased capacity for the certification of the performance and safety of medical devices, for healthcare professionals and the public.
Animal by-products (ABPs) you can use to make pet food, how to provide samples, and how to package your products.
Apply to become an approved exporter (AE) and operate legally under the approval.
Criteria that qualifications in the statutory entitlements offer need to meet alongside the common funding approval criteria.
Consultation on whether to update the GB road vehicle type approval scheme to accept certain new safety and environmental standards.
First published during the 2022 to 2024 Sunak Conservative government
The approach the MHRA intends to take for products approved or pending in decentralised procedure (DCP) or mutual recognition procedures (MRP).
How cars are inspected when they're being approved under the Individual Vehicle Approval (IVA) scheme to make sure they're safe to be used.
Application form ACD: HM Land Registry approval of standard form of charge deed, and allocation of the official HM Land Registry reference.
The Medicines and Healthcare products Regulatory Agency (MHRA) has designated three new UK Approved Bodies, almost doubling the UK’s capacity to certify medical devices, supporting faster certification of safe and effective medical devices for healthcare professionals and the public.
The process independent special providers need to follow to be considered for entry onto the list of approved institutions.
Find out how to apply to operate premises as an excise warehouse, how to renew or make changes to your approval and what happens if HMRC cancel your approval.
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