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Open tenders / Medical supplies & equipment

Planned procurement · Notice 090106-2026

NEYPPC Pharmacy - Unlicensed Imported Medicines (wave 2)

Leeds Teaching Hospitals NHS Trust

Value
£36.1m
Stage
Early notice
Where
UK-wide
Lots
1
Suitable for SMEs
Yes, says the buyer
Contract
1 May 2027 – 31 Dec 2028

In plain English

NHS pharmacy buyers across the North East and Yorkshire want to set up a list of approved suppliers for unlicensed imported medicines (products licensed abroad but not in the UK), including over-labelling and translation of packaging. The arrangement runs from 1 May 2027 to 31 December 2028 and is valued at about £36.1m.

Good fit for: Licensed pharmaceutical importers and specials/unlicensed medicines wholesalers.

Watch out: Must hold all relevant MHRA licences, authorisations and approvals to import, distribute and supply unlicensed medicines in the UK; Must demonstrate compliance with Good Manufacturing Practice (GMP) and Good Distribution Practice (GDP); Supply must comply with Regulation 167 of the Human Medicines Regulations 2012; Products and suppliers face comprehensive quality, risk and commercial assessment

Written with AI from the official notice. Check the notice before relying on it.

What the buyer says

The North East and Yorkshire NHS Pharmaceutical Purchasing Consortium intends to establish a framework agreement for the supply of Unlicensed Imported Medicines on behalf of NHS organisations and other eligible public sector bodies. The framework will provide access to a defined range of unlicensed imported medicines, including products requiring over-labelling and translation. These medicines do not hold a UK Marketing Authorisation but are licensed in their country of origin and may be imported and supplied in accordance with Regulation 167 of the Human Medicines Regulations 2012 where a patient's clinical needs cannot be met by a suitable licensed alternative. Suppliers will be required to hold all relevant MHRA licences, authorisations and approvals necessary to import, distribute and supply unlicensed medicines within the UK, and to demonstrate compliance with applicable Good Manufacturing Practice (GMP) and Good Distribution Practice (GDP) standards. The framework will provide participating organisations with access to safe, compliant and quality-assured products through a robust and competitive procurement arrangement. Products and suppliers will be subject to comprehensive quality, risk and commercial assessment to support regulatory compliance, supply chain resilience, continuity of patient care and value for money across the NHS.

Procedure: Competitive flexible procedure. Published 23 Sep 2026.

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