Accreditations & Standards

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ISO 17025:2017 Accredited

General requirements for the competence of testing and calibration laboratories. Our scope covers all major chromatography and mass spectrometry methods.

cGMP / cGLP Compliant

We adhere to Current Good Manufacturing Practice and Good Laboratory Practice regulations enforced by the FDA.

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Data Integrity

21 CFR Part 11 compliant data systems ensuring record security, audit trails, and electronic signature validity.

Audit-Ready, Always.

We understand that your data submission to regulatory bodies depends on our compliance. That's why we maintain a state of constant readiness.

Instrument Qualification (IQ/OQ/PQ)

Every instrument undergoes rigorous qualification protocols before processing a single sample.

Method Validation

Methods validated for specificity, linearity, range, accuracy, precision, LOD/LOQ, and robustness.

Internal Audits

Quarterly internal audits to identify and rectify any potential non-conformances proactively.

Proficiency Testing

Regular participation in inter-laboratory comparison schemes to benchmark performance.

CERTIFICATE OF ACCREDITATION