Purchase of Rare or Inherited Disease Test Directory testing for Welsh patients
key details
| Status | complete |
|---|---|
| Category (CPV) | 33910000 |
| Region | Wales |
| Procedure | limited |
| OCID | ocds-h6vhtk-0459eb |
Award
| Supplier | Value | Date | Status |
|---|---|---|---|
| CeGaT GmbH | · | · | active |
description
In-line with All Wales Medical genomic Service’s (AWMGS) commissioning model, AWMGS will procure from CeGaT whole exom sequencing (WES) for trio or singleton virtual panel analysis, MLPA and single gene testing for patients where this testing cannot be accessed within the NHS E laboratory network. This genetic testing will ensure equity of access to genomic testing for Welsh patients and meet their need to seek a timely genetic diagnosis for their rare or inherited disease.
documents
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notice history
1 notice published against this procurement.
| Published | Type | Regime | Notice |
|---|---|---|---|
| 15 May 2024 | Voluntary ex-ante transparency (F15) | Earlier regulations | 015493-2024 |
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source
Published on Sell2Wales. Contact details for named individuals are not reproduced on this site.