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Pharmacogenomic (Pgx) Testing Service Tender - 143509335

The ULSTER UNIVERSITY has issued a Tender notice for the procurement of a Pharmacogenomic (Pgx) Testing Service in the United Kingdom. This Tender notice was published on 18 Jun 2026 and is scheduled to close on 24 Jun 2026, with an estimated Tender value of Refer Document. Interested bidders can access detailed Tender information, eligibility criteria, and complete bidding documents by referencing TOT Ref No. 143509335, while the tender notice number is 6532577 and Registering on the platform.

Expired Tender

Procurement Summary

Country: United Kingdom

Summary: Pharmacogenomic (Pgx) Testing Service

Deadline: 24 Jun 2026

Posting Date: 18 Jun 2026

Other Information

Notice Type: Tender

TOT Ref.No.: 143509335

Document Ref. No.: 6532577

Competition: ICB

Financier: Self Financed

Purchaser Ownership: Public

Tender Value: Refer Document

CPV Classification

85140000 - Miscellaneous health services
85145000 - Services provided by medical laboratories
85148000 - Medical analysis services
71900000 - Laboratory services

Purchaser's Detail

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Tender Details

The project wishes to appoint a suitable laboratory or multiple labs to supply an end-to-end genomic testing service which provides genomic variant data for n=4, 854 participants in Northern Ireland (NI) and Ireland. Specifically, the areas where the project will recruit participants from of relevance to this tender includes counties Londonderry, Tyrone in Northern Ireland and counties Donegal and Sligo in Ireland. The iMPROVE project will operate on the basis of a research implementation study which aims to integrate pharmacogenomic testing into a patient-centred medicines optimisation care pathway in GP practices across the project regions. The new integrated care pathway will be led by GP practice pharmacists with a focus on medicines optimisation to improve outcomes, removing inappropriate and ineffective treatments and adverse drug event risk reduction. Medications for pain, depression, anxiety and cardiovascular disease are the most prescribed drugs which also display considerable variation in efficacy, in part due to single nucleotide polymorphisms (SNPs) in genes which can alter efficient drug metabolism. A laboratory service is required to transport participant samples from GP sites, test for a finite list of SNPs which alter the rate of metabolism of a constrained list of prescribed medications including opioids, SSRI-s, PPI-s, statins and Clopidgrel.
Notice identifier : 2026/S 000-057137
CPV classifications: 85140000 - Miscellaneous health services85145000 ...

Documents

 Tender Notice


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