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Information relating to parallel imports and the implementation of the Windsor Framework.
Parallel import licences granted in 2024
Obligated packaging producers must register and meet their waste packaging recycling responsibilities.
Definitive fees charged for applications under Schedule 7 of the Veterinary Medicines Regulations 2013.
This page includes summaries of the winning bids for the Future RAN (FRANC) competition
Apply to manufacture Extemporaneous preparations, Autogenous vaccines, authorisations for Equine Stem Cell Centre (ESCCA) or Non-Food Animal Blood Bank (NFABBA).
How to use a quasi-experimental study to evaluate your digital health product.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
For MAHs, manufacturers, wholesalers, retailers (including vets) and feed businesses on the manufacture and movement of veterinary medicines in relation to the NI Protocol and Brexit.
A wholesale dealer in Great Britain may import Qualified Person certified medicines from the European Economic Area if certain checks are made by the ‘Responsible Person (import)’
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Apply for protection against infringements of intellectual property rights on imports into and exports out of the UK.
We work with organisations across the UK that produce radioactive waste.
This guide sets out who has to apply for a permit, how to apply and explains the other rules covering travel to Antarctica.
Apply for an authorisation to manufacture authorised veterinary medicines and medicines marketed under the Exemptions for Small Pet Animals.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
An overview of the work the IPO is undertaking in relation to Standard Essential Patents.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
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