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Actions that parallel exporters to the EEA and intellectual property rights holders need to take.
How to get a parallel import licence for your medicine in the UK, including pharmacovigilance requirements and submitting your application.
Information for wholesale dealer licence holders about the medicines put on the UK market for UK patients that they cannot export or hoard.
Parallel import licences granted in 2024
The process to convert Parallel Distribution Notices (PDNs) into Parallel Import Licences (PILs)
Guidance for the pharmaceutical industry on how to apply for an authorisation to place a veterinary medicine on the UK market or part of, or to expire one.
Parallel import (PLPI) licences granted since January 2014.
This guidance explains the Counter Proliferation Programme objectives for the financial year 2024 to 2025 and how to apply through the project bidding process.
Information relating to parallel imports and the implementation of the Windsor Framework.
What driving instructors should do to carry out realistic mock driving tests, including what needs to be in the test, assessing faults and recording the result.
How to use a crossover randomised controlled trial to evaluate your digital health product.
Parallel import licences granted in 2023
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
These published standards relate to a number of KPIs in the VMD Deliverables and KPI document.
How to get plant breeders' rights and what protection it gives your plant varieties.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
This guidance sets out how the MHRA is handling centralised applications that were still pending on 1 January 2021.
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