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Medical genetic testing kits

Buyer: NHS Wales Shared Services Partnership-Procurement Services (hosted by Velindre University NHS Trust)

Deadline
Not available — this notice may describe a possible future opportunity.
Region
Not specified
Value
£96,000
Type
Award,contract
SME fit
Duration

Description

The All Wales Medical Genomics Service (AWMGS) has routinely utilised Multiplex Ligation-Dependent Probe Amplification (MLPA) as a diagnostic tool for identifying Copy Number Variations (CNVs)—including deletions and duplications—across a range of genetic disorders. This testing supports clinical decision-making and patient treatment strategies.MLPA technology involves the use of oligonucleotide probe pairs that hybridise to specific DNA sequences within target genes. When both probes bind adjacently at a site of interest, they are ligated and subsequently amplified via Polymerase Chain Reaction (PCR). The amplified DNA fragments are then separated by capillary electrophoresis and analysed to detect CNVs.Since its inception, AWMGS has exclusively sourced MLPA probes and reagents from MRC Holland, a Netherlands-based supplier recognised for its specialised products in molecular diagnostics.

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Key details
CPV category
Procurement method
Below threshold - without competition
Published
29 Sep 2025 15:15
VCSE suitable
Reference
OCID
ocds-h6vhtk-05a434
Notice ID
CAV-DCO (25-26) 96
In our database since
18 Aug 2026