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Instrument Implementation & Verifications support

Instrument Verification for UKAS accreditation

In Collaboration with IVD manufacturers our team complete the verification process of any instrument installed for clinical use.

Services provided as part of the instrument installation process.

Stage 1. Manufacturer Engineers will conduct installation (IQ).
Stage 2. Manufacturer Product specialist performs operational qualification (OQ).
Stage 3. Our UKAS support team will complete the performance qualification (PQ) and write report compliant to client's local protocol whilst ensuring compliance to to ISO15189, 2022 Verification requirements; 7.3.2 Verification of examination methods.

Why choose this service

We have a range sample types in our biobank and extensive clinical support to ensure verification of examination methods is fully compliant to ensure the validity of results pertinent to clinical decision making.

PQ will be fully completed ready for assessment from as little as 7 days saving your organization valuable time.

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Instrument Implementation & Verifications support

Instrument Verification for UKAS accreditation

Why choose this service

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