Regulatory Compliance Services for Medical Devices

Scope of works

Support in respect of the achievement of ISO 13485 certification, a critical requirement for the development and deployment of higher-risk software and AI medical devices, including the planned Probabilistic AI Triage product. The service is essential to ensure continuity of expertise, retain critical organisational knowledge built over the last two years, and avoid delays to regulatory, quality and medical device activities. The proposed arrangement will provide business continuity, support the continued maturity of the Quality Management System,

Type

Contract award

Contract Award

Sector

Healthcare & Medical

Procedure

Below threshold - without competition

Classification

Not published at source

Original notice

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Source provenance (1)

Every portal notice that contributed to this record, with the values each one published. Where portals disagree, the originating notice is the published record.

Key dates

1. Published at source23 Sept 2026
2. Submission deadline—