United Kingdom7 days leftOpen

Next Generation Sequencing Testing (NGS)

Tender Overview

LOCATION

Gloucestershire, Wiltshire and Bristol/Bath area, United Kingdom

VALUE

£660,000

DEADLINE

February 09, 2026 at 12:00

CATEGORY

Other

CPV CODE

72225000

REFERENCE

002096-2026

Project Timeline

Contact Information

View Original

Original Tender Description

NHS Blood and Transplant (NHSBT) are seeking a provider for Next Generation Sequencing (NGS) QC testing requirements for the Cellular and Molecular Therapies (CMT) directorate, namely the Clinical Biotechnology Centre (CBC). CBC handle a number of products in the production of Advanced Therapeutic Investigational Medicinal Products (ATMPs) and starter material master cell banks (MCBs). These require NGS QC testing services that meet specific regulatory requirements.
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MANDATORY EXCLUSION GROUNDS

  • No specific mandatory exclusion grounds are detailed in the provided information.

ELIGIBILITY REQUIREMENTS

  • The provider must possess an EU Good Manufacturing Practice (GMP) Licence.
  • The provider must adhere to specific regulatory standards relevant to NGS QC testing services for Advanced Therapeutic Investigational Medicinal Products (ATMPs) and starter material master cell banks (MCBs).
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TECHNICAL CAPABILITY REQUIREMENTS

  • The provider must be capable of performing Next Generation Sequencing (NGS) QC testing services.
  • The provider must be able to provide NGS QC testing services relevant to the needs of the Clinical Biotechnology Centre (CBC), which handles Advanced Therapeutic Investigational Medicinal Products (ATMPs) and starter material master cell banks (MCBs).
  • The provider's NGS QC testing services must meet specific regulatory requirements applicable to ATMPs and MCBs.
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FINANCIAL REQUIREMENTS

  • No specific financial requirements for bidders are detailed in the provided information.
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SUBMISSION REQUIREMENTS

  • Bids must be submitted by the deadline of 2026-02-09 12:00:00.

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PDF
Official PDF Version
PDF002096-2026_official.pdf
Summary:
NHS Blood and Transplant seeks a provider for Next Generation Sequencing (NGS) QC testing services for its Clinical Biotechnology Centre, requiring an EU Good Manufacturing Practice (GMP) Licence and adherence to specific regulatory standards.

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67
Good

Tender Quality Score

This tender is critically incomplete due to the complete absence of tender documents and evaluation criteria, making it impossible for potential bidders to prepare a compliant offer. While the service description is clear, the lack of fundamental procurement information severely undermines its quality and fairness.

Score Breakdown

Legal Compliance100/100

Legal compliance is severely compromised by the absence of tender documents, specific mandatory exclusion grounds, and crucially, evaluation criteria. A competitive procedure without clear evaluation criteria is fundamentally flawed and lacks transparency.

Absence of tender documents, which are essential for legal compliance and bidder understanding.
Missing specific mandatory exclusion grounds, which are standard legal requirements.
Clarity40/100

The description of the required service (NGS QC testing for ATMPs/MCBs) is clear. However, the overall clarity of the tender is extremely poor due to the complete lack of supporting documents, detailed specifications, and terms and conditions. The broad CPV code and missing NUTS code also reduce clarity.

Complete absence of tender documents, leading to extreme lack of clarity on requirements and process.
Broad CPV code ('System quality assurance assessment and review services') may not accurately reflect the specialized NGS testing, potentially confusing bidders.
Completeness83/100

The tender is critically incomplete. Key elements such as full tender documents, evaluation criteria, specific mandatory exclusion grounds, and financial requirements for bidders are entirely missing. This renders the tender non-functional.

No tender documents attached or content available, making the tender fundamentally incomplete.
Missing evaluation criteria, which are essential for any competitive procurement.
Fairness60/100

Fairness is severely compromised by the absence of evaluation criteria, making the assessment process opaque and subjective. The requirement for an 'EU Good Manufacturing Practice (GMP) Licence' for a UK-based organization (NHSBT) could be seen as potentially tailoring the tender or unduly limiting competition if not thoroughly justified and clarified in full documentation.

Absence of evaluation criteria makes the tender process unfair and non-transparent for bidders.
The requirement for an 'EU Good Manufacturing Practice (GMP) Licence' for a UK contracting authority could potentially limit competition or be perceived as tailoring if not clearly justified and explained in the context of post-Brexit regulations and market access.
Practicality40/100

The tender is highly impractical for both the contracting authority and potential bidders. Bidders cannot prepare a meaningful submission without any tender documents, detailed requirements, or evaluation criteria. This will likely result in very few, if any, compliant bids.

Bidders cannot practically prepare a compliant and competitive bid without any tender documents or evaluation criteria.
Data Consistency100/100

Based on the limited information provided, the data is internally consistent. However, the complete absence of tender documents means there is no further content to assess for consistency.

Sustainability0/100

There is no mention of green procurement, social criteria, or innovation focus, indicating a lack of consideration for broader sustainability objectives in this tender.

No green procurement criteria specified.
No social criteria specified.

Strengths

Clear title, reference number, and contracting organization.
Detailed description of the required service (NGS QC testing for ATMPs/MCBs).
Estimated value and contract duration are provided.
Procedure type (Competitive flexible procedure) is specified.

Concerns

Critical absence of all tender documents, making the tender non-functional.
Missing evaluation criteria, which undermines fairness, transparency, and legal compliance.
Lack of specific mandatory exclusion grounds and financial requirements for bidders.
The 'EU Good Manufacturing Practice (GMP) Licence' requirement for a UK entity could limit competition or be perceived as tailoring.
Broad CPV code and missing NUTS code reduce clarity and market reach.

Recommendations

1. Immediately publish all comprehensive tender documents, including detailed specifications, terms and conditions, and explicit evaluation criteria.
2. Clearly define and justify all eligibility requirements, particularly the 'EU Good Manufacturing Practice (GMP) Licence', in the context of the contracting authority's location and regulatory landscape.
3. Review and update the CPV code to be more specific to advanced biotechnology or laboratory testing services, and specify the NUTS code or geographical scope.

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Tender Quality Score
67/ 100 · Good

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