RFP QuestBeta
Awarded · ResultStage · contract

De Montfort University

1313(REISSUE) Development of a new Graphical Interface and Associated Hardware and Software for the Rober NoDec Wizard

Business ServicesCPV 79415200 79933000
ValueValue not published
Awarded19 Sept 2019
Published6 Sept 2019
RegionEast Midlands
Outcome — awarded

This is a contract result notice, not an open opportunity. Details from the official award data.

The brief

De Montfort University (DMU) invites bids from suitably experienced providers for the prototype of a full graphical interface system and required electronics and software interface for the NoDec Wizard for the company Rober Ltd.

This must be available by 13th November 2019 for the MEDICA exhibition which commences on the 18th November 2019.

The evaluation must be undertaken by an ISO 13485 approved (for design and manufacture) organisation and must conform to current Medical Device Directives (MDD) and future Medical Device Requirements (MDR).

DMU's detailed requirements are defined within the Specification.

All other information relating to Award Criteria, evaluation and the full specification etc can be found within our RfQdocument for this procurement loaded on the In-Tend e-tendering portal https://in-tendhost.co.uk/demontfort/aspx/Home

Key requirements

What the supplier must deliver

01

This must be available by 13th November

This must be available by 13th November 2019 for the MEDICA exhibition which commences on the 18th November 2019.

02

The evaluation must be undertaken by

The evaluation must be undertaken by an ISO 13485 approved (for design and manufacture) organisation and must conform to current Medical Device Directives (MDD) and future Medical Device Requirements (MDR).

Derived from the notice text — always confirm against the original documents.

The gates

What this notice demands of you

1 named in obligation language, 0 mentioned. Each one is quoted from the notice.

ISO 13485 (medical devices)says mustStandards you certify to
The evaluation must be undertaken by an ISO 13485 approved (for design and manufacture) organisation and must conform to current Medical Device Directives (MDD) and future Medical Device Requirements (MDR).

Matched against the notice text, so this is a floor — the tender pack will demand things the notice never mentions. “Says must” means the quoted sentence itself used obligation language; anything ambiguous is left as a mention.

Buyer intelligence

Make the case to bid

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Source & provenance
OCID
6b8b059f-355e-4050-901d-d4b0a3296dd1
Stage
contract · Contract
Source
Contracts Finder
Buyer ref
1313/1
View the original notice on Contracts Finder

Contains public sector information licensed under the Open Government Licence v3.0. Source data © Crown copyright.

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