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Purchase of Rare or Inherited Disease Test Directory testing for Welsh patients

key details

Statuscomplete
Category (CPV) 33910000
RegionWales
Procedurelimited
OCIDocds-h6vhtk-0459eb

Award

SupplierValueDateStatus
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.

PublishedTypeRegimeNotice
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.