Medicines: apply for a parallel import licence
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How to get a parallel import licence for your medicine in the UK, including pharmacovigilance requirements and submitting your application.
Adapted edition
- Document type
- Reference Guide
- Format
- DOCX
- Pages
- 8
- Language
- English
- Version
- 1.0
- Updated
- 2026-09-17
- Category
- Safety & operations
- Licence
- Open Government Licence v3.0
Description
How to get a parallel import licence for your medicine in the UK, including pharmacovigilance requirements and submitting your application. Consult the original guidance for current legal and operational details.
Contents
- Parallel import licence application categories
- Parallel import (simple)
- Parallel import (complex)
- Parallel import (standard)
- Parallel Imports following the agreement of the Windsor Framework
- Falsified Medicines Directive: Requirements for Parallel Imports
- Submit your parallel import licence application
- Documents for submission
- Sample scan submission
- Packaging materials
- Labelling Artwork Submission
- Patient Information Leaflets (PILs)
- User testing for readability of patient information leaflets
- Company Functions involved in parallel importing
- Suppliers' list declaration
- Assessment process - One 'RFI' Rule
Source and licence
Medicines and Healthcare products Regulatory Agency
AttributionMedicines and Healthcare products Regulatory Agency, ‘Medicines: apply for a parallel import licence’ (updated 26 August 2026), reused under the Open Government Licence v3.0.
ChangesNeutral text-only adaptation from the official GOV.UK Content API body: headings, paragraphs, ordered and unordered list items and clickable source-link destinations in an appendix preserved. Images, logos, page design, accessible-format request widgets and linked attachments excluded; normalised whitespace, invisible format marks and typography.
Version history
- v1.017/09/2026