PMRA DocumentPMRA wholesale premises requirements (prescription link)
Currentness under review. Whether this instrument remains applicable is under review. Consult the later instruments and source context below before relying on it.
Minimum Requirements for Prescription Wholesale Pharmacy — prescription copy is published by Pharmacy and Medicines Regulatory Authority. This document is identified by its title; no separate official document code is recorded.
- Instrument
- Document
- Full name
- PMRA wholesale premises requirements (prescription link)
- Category
- Registration
- Source publication
- English
- Readable HTML
- 1 language version
- Published
- —
- Effective
- —
Open a language version
Each version has stable passage anchors for direct citations and highlighting. The readable text is generated from an authority source and does not replace the legally controlling publication.
Minimum Requirements for Prescription Wholesale Pharmacy — prescription copy
Complete three-page PMRA premises guidance, retained with every original page image. Sections D and F expressly cover source/stock records and storage/security for allied substances as well as pharmaceutical products. It also specifies premises space, shelving, temperature control, segregation of recalled/expired/rejected goods, references and staffing. The original title reads PRESCRIPTION WHOLESALE PHARMCY in both separately supplied copies. This copy is linked and named prescription. A4/A5 specify a pharmacist; section B repeats DOCUMENTS TO BE SUBMITTED above premises conditions. These original differences from the copy linked as non-prescription are preserved, without inferring a controlled revision or legal replacement. The three-month locum provision concerns staffing subject to authority approval, not device variation review. No controlled document identifier or issue/effective date appears, and the upload directory is not used as a legal date. The document remains currentness-unverified and excluded from default current discovery. This is guidance for the stated pharmacy-premises context; it does not replace the missing dedicated medical-device-wholesaler requirements or establish a general standalone-device/IVD procedure.
This document is identified by its title; no separate official document code is recorded. Always confirm the current consolidated text and transition provisions with the official source before filing.