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Hysbysiad o Gontract

Research Environment Clinical Data Platform

  • Cyhoeddwyd gyntaf: 19 Ebrill 2019
  • Wedi'i addasu ddiwethaf: 19 Ebrill 2019

Nid yw'r prynwr yn defnyddio'r wefan hon i weinyddu'r hysbysiad.

I gofnodi eich diddordeb neu gael gwybodaeth neu ddogfennau ychwanegol, darllenwch y cyfarwyddiadau yn Nhestun Llawn yr Hysbysiad. (NODER: Nid oes angen ymateb i Hysbysiadau Dyfarnu Contractau a Hysbysiadau Gwybodaeth Ymlaen Llaw fel arfer)

Cynnwys

Crynodeb

OCID:
Cyhoeddwyd gan:
Genomics England Limited
ID Awudurdod:
AA23344
Dyddiad cyhoeddi:
19 Ebrill 2019
Dyddiad Cau:
24 Mai 2019
Math o hysbysiad:
Hysbysiad o Gontract
Mae ganddo ddogfennau:
Nac Ydi
Wedi SPD:
Nac Ydi
Mae ganddo gynllun lleihau carbon:
AMH

Crynodeb

As part of 100 000 Genome Project, Genomics England established a secure Research Environment (RE) to contribute to the realisation of Genomics England’s target benefits which are:

— patient benefit,

— new scientific insights and discovery,

— accelerating the uptake of genomic medicine in the NHS,

— stimulating and enhancing UK industry and investment, and

— increasing public knowledge and support for genomic medicine.

Design, development and operation of the RE are driven by its objective to “provide a secure and collaborative workspace that enables researchers and industry to perform genomic data analysis to accelerate scientific discovery.”

Below outlines the scope of the RE and the target capabilities that are being delivered as part of a programme of work. A brief description of the capabilities that are to be delivered are provided below.

People

— staff appropriately skilled to implement, maintain and support the required data platforms,

— recruitment and staff development that maintains the required skills within Genomics England,

— organisational structures and resources required to support the effective operation and improvement of the data platforms.

Policy and Process

— solutions that drive a standardised approach to data governance, consent practises, data release and other relevant policies and processes,

— solutions that enable effective management of data quality,

— policies and processes that enable users to work securely, efficiently and effectively in the Research Environment.

Technology

— software and infrastructure that meet functional, security, governance, capacity and performance requirements of the research environment,

— technology providing the usability, availability, accessibility, flexibility, interoperability and scalability required by both academic and commercial users.

A key component of the RE is a clinical data platform. The platform will accommodate unstructured, semi-structured and structured data.

Over and above the platform, there is a requirement for support services.

Testun llawn y rhybydd

Hysbysiad contract

Adran I: Endid contractio

I.1) Enw a chyfeiriad

Genomics England Ltd

Dawson Hall, Charterhouse Square

London

EC1M 6BQ

UK

Person cyswllt: Paul Nicholson, Procurement Lead

Ffôn: +44 2078825030

E-bost: paul.nicholson@genomicsengland.co.uk

NUTS: UKI

Cyfeiriad(au) rhyngrwyd

Prif gyfeiriad: https://www.genomicsengland.co.uk

I.3) Cyfathrebu

Mae'r dogfennau caffael ar gael ar gyfer mynediad uniongyrchol anghyfyngedig a llawn, yn rhad ac am ddim ar:

https://genomicsengland.bravosolution.co.uk/genomicsengland/web/login.html


Gellir cael gwybodaeth ychwanegol o'r cyfeiriad uchod


Rhaid anfon tendrau neu geisiadau i gymryd rhan yn electronig at:

https://genomicsengland.bravosolution.co.uk/genomicsengland/web/login.html


Rhaid anfon tendrau neu geisiadau i gymryd rhan i'r cyfeiriad uchod:


I.4) Y math o awdurdod contractio

Corff a lywodraethir gan gyfraith gyhoeddus

I.5) Prif weithgaredd

Arall: Genomics

Adran II: Gwrthrych

II.1) Cwmpas y caffaeliad

II.1.1) Teitl

Research Environment Clinical Data Platform

Cyfeirnod: GeL-RE-004-18

II.1.2) Prif god CPV

72222300

 

II.1.3) Y math o gontract

Gwasanaethau

II.1.4) Disgrifiad byr

As part of 100 000 Genome Project, Genomics England established a secure Research Environment (RE) to contribute to the realisation of Genomics England’s target benefits which are:

— patient benefit,

— new scientific insights and discovery,

— accelerating the uptake of genomic medicine in the NHS,

— stimulating and enhancing UK industry and investment, and

— increasing public knowledge and support for genomic medicine.

Design, development and operation of the RE are driven by its objective to “provide a secure and collaborative workspace that enables researchers and industry to perform genomic data analysis to accelerate scientific discovery.”

II.1.6) Gwybodaeth am lotiau

Mae’r contract hwn wedi’i rannu’n lotiau: Na

II.2) Disgrifiad

II.2.2) Cod(au) CPV ychwanegol

48000000

48100000

71600000

71621000

72000000

72212100

72262000

II.2.3) Man cyflawni

Cod NUTS:

UKI


Prif safle neu fan cyflawni:

London

II.2.4) Disgrifiad o’r caffaeliad

As part of 100 000 Genome Project, Genomics England established a secure Research Environment (RE) to contribute to the realisation of Genomics England’s target benefits which are:

— patient benefit,

— new scientific insights and discovery,

— accelerating the uptake of genomic medicine in the NHS,

— stimulating and enhancing UK industry and investment, and

— increasing public knowledge and support for genomic medicine.

Design, development and operation of the RE are driven by its objective to “provide a secure and collaborative workspace that enables researchers and industry to perform genomic data analysis to accelerate scientific discovery.”

Below outlines the scope of the RE and the target capabilities that are being delivered as part of a programme of work. A brief description of the capabilities that are to be delivered are provided below.

People

— staff appropriately skilled to implement, maintain and support the required data platforms,

— recruitment and staff development that maintains the required skills within Genomics England,

— organisational structures and resources required to support the effective operation and improvement of the data platforms.

Policy and Process

— solutions that drive a standardised approach to data governance, consent practises, data release and other relevant policies and processes,

— solutions that enable effective management of data quality,

— policies and processes that enable users to work securely, efficiently and effectively in the Research Environment.

Technology

— software and infrastructure that meet functional, security, governance, capacity and performance requirements of the research environment,

— technology providing the usability, availability, accessibility, flexibility, interoperability and scalability required by both academic and commercial users.

A key component of the RE is a clinical data platform. The platform will accommodate unstructured, semi-structured and structured data.

Over and above the platform, there is a requirement for support services.

II.2.5) Meini prawf dyfarnu

Nid pris yw’r unig faen prawf dyfarnu a dim ond yn y dogfennau caffael y mae’r holl feini prawf wedi’u nodi

II.2.7) Hyd y contract, y cytundeb fframwaith neu’r system brynu ddynamig

Hyd mewn misoedd: 60

Gall y contract hwn gael ei adnewyddu: Ydy

Disgrifiad o’r adnewyddiadau:

Initial contract length of 36 months with 2 options to renew for 12 month periods making the total possible contract length 60 months.

II.2.9) Gwybodaeth am y cyfyngiadau ar nifer yr ymgeiswyr a gaiff eu gwahodd

II.2.10) Gwybodaeth am amrywiadau

Derbynnir amrywiadau: Na

II.2.11) Gwybodaeth am opsiynau

Opsiynau: Na

II.2.13) Gwybodaeth am Gronfeydd yr Undeb Ewropeaidd

Mae'r broses gaffael yn gysylltiedig â phrosiect a/neu raglen a ariennir gan gronfeydd yr Undeb Ewropeaidd: Na

Section III: Gwybodaeth gyfreithiol, economaidd, ariannol a thechnegol

III.1) Amodau ar gyfer cymryd rhan

III.1.2) Statws economaidd ac ariannol

Meini prawf dethol fel y’u nodir yn y dogfennau caffael


III.1.3) Gallu technegol a phroffesiynol

Meini prawf dethol fel y’u nodir yn y dogfennau caffael


III.2) Amodau sy’n gysylltiedig â’r contract

Section IV: Gweithdrefn

IV.1) Disgrifiad

IV.1.1) Y math o weithdrefn

Gweithdrefn gyfyngedig

IV.1.8) Gwybodaeth am Gytundeb Caffael y Llywodraeth (GPA)

The procurement is covered by the Government Procurement Agreement: Na

IV.2) Gwybodaeth weinyddol

IV.2.1) Cyhoeddiad blaenorol mewn perthynas â’r weithdrefn hon

Rhif yr hysbysiad yn OJ S:

2018/S 207-472572

IV.2.2) Terfyn amser i dendrau neu geisiadau i gymryd rhan ddod i law

Dyddiad: 24/05/2019

Amser lleol: 12:00

IV.2.3) Dyddiad amcangyfrifedig ar gyfer anfon gwahoddiadau i dendro neu i gymryd rhan at yr ymgeiswyr a ddewiswyd

Dyddiad: 07/06/2019

IV.2.4) Ym mha iaith/ieithoedd y gellir cyflwyno tendrau neu geisiadau i gymryd rhan

EN

IV.2.6) Yr isafswm cyfnod gofynnol i’r sawl sy’n tendro gynnal y tendr

Hyd mewn misoedd: 3  (o’r dyddiad a nodwyd i dendr ddod i law)

Section VI: Gwybodaeth ategol

VI.1) Gwybodaeth am ailddigwydd

Caffaeliad cylchol yw hwn: Na

VI.2) Gwybodaeth am lifau gwaith electronig

Derbynnir anfonebau electronig

Defnyddir taliadau electronig

VI.3) Gwybodaeth ychwanegol

The Contracting Authority expressly reserves the right

(i) not to award any contract as a result of the procurement process commenced by publication of this notice; and

(ii) to make whatever changes it may see fit to the content and structure of the tendering competition; and in no circumstances will the Contracting Authority be liable for any costs incurred by the candidates. Any expenditure, work or effort undertaken prior to contract award is accordingly a matter solely for the commercial judgement of potential suppliers.

(a) Genomics England reserves the right at any stage to reject or disqualify or revise the pre-qualified status of any tenderer who:

1) Provides information or confirmations which later prove to be untrue or incorrect; and/or

2) Does not submit a tender in accordance with the requirements of the tender document or as otherwise directed by Genomics England during the procurement process; and/or

3) Fulfils any one or more of the criteria detailed in the Public Contracts Regulations 2016 pertaining to Mandatory Exclusions.

(b) further information on Genomics England may be found at https://www.genomicsengland.co.uk/

(c) all discussions and meetings will be conducted in English;

(d) tenders and supporting documents must be priced in GBP and all payments under the contract will be made in sterling;

(e) Genomics England may interview any or all economic operators who express an interest in tendering for this work.

VI.4) Gweithdrefnau adolygu

VI.4.1) Corff adolygu

High Court

London

UK

VI.5) Dyddiad anfon yr hysbysiad hwn

17/04/2019

Codio

Categorïau nwyddau

ID Teitl Prif gategori
71621000 Gwasanaethau dadansoddi neu ymgynghori technegol Gwasanaethau dadansoddi
72262000 Gwasanaethau datblygu meddalwedd Gwasanaethau sy’n gysylltiedig â meddalwedd
72212100 Gwasanaethau datblygu meddalwedd penodol i ddiwydiant Gwasanaethau rhaglennu meddalwedd rhaglenni
71600000 Gwasanaethau profi, dadansoddi ac ymgynghori technegol Gwasanaethau pensaernïol, adeiladu, peirianneg ac archwilio
72222300 Gwasanaethau technoleg gwybodaeth Systemau gwybodaeth neu wasanaethau adolygu a chynllunio technoleg strategol
72000000 Gwasanaethau TG: ymgynghori, datblygu meddalwedd, y Rhyngrwyd a chymorth Gwasanaethau Cyfrifiadurol a Chysylltiedig
48100000 Pecyn meddalwedd penodol i ddiwydiant Systemau pecynnau meddalwedd a gwybodaeth
48000000 Systemau pecynnau meddalwedd a gwybodaeth Gwasanaethau Cyfrifiadurol a Chysylltiedig

Lleoliadau Dosbarthu

ID Disgrifiad
100 DU - I gyd

Cyfyngiadau Rhanbarthol ar y Rhybuddion

Mae’r prynwr wedi cyfyngu’r rhybuddion ar gyfer yr hysbysiad hwn i gyflenwyr yn y rhanbarthau canlynol.

ID Disgrifiad
Nid oes cyfyngiadau ar y rhybuddion ar gyfer yr hysbysiad hwn.

Ynglŷn â'r prynwr

Prif gyswllt:
paul.nicholson@genomicsengland.co.uk
Cyswllt gweinyddol:
N/a
Cyswllt technegol:
N/a
Cyswllt arall:
N/a

Gwybodaeth bellach

Dyddiad Manylion
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0800 222 9004

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