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Guidance for the pharmaceutical industry on applying for a marketing authorisation for parallel import (MAPI).
How to get a parallel import licence for your medicine in the UK, including pharmacovigilance requirements and submitting your application.
The process to convert Parallel Distribution Notices (PDNs) into Parallel Import Licences (PILs)
Actions that parallel exporters to the EEA and intellectual property rights holders need to take.
Parallel import licences granted in 2024
Definitive fees charged for applications under Schedule 7 of the Veterinary Medicines Regulations 2013.
Sets out medicines that cannot be exported from the UK or hoarded because they are needed for UK patients.
Parallel import (PLPI) licences granted since January 2014.
Information relating to parallel imports and the implementation of the Windsor Framework.
Explainer for the pharmaceutical industry on the ongoing implementation of the Veterinary Medicines Regulation relating to applications and authorisations for veterinary medicines.
The actions to take for sourcing medicines in different circumstances.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
This page includes summaries of the winning bids for the Future RAN (FRANC) competition
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
Guidance on plan-making.
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