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Galbraith Laboratories has been awarded accreditation by the American Association for Laboratory Accreditation (A2LA). This accreditation ensures compliance of our internal quality system, technical staff, and calibration protocols to ISO/IEC 17025:2005 general requirements for the competence of testing and calibration laboratories. The scope of accreditation may be viewed at www.galbraith.com/iso17025.pdf.
Galbraith operates as a Good Laboratory Practices (GLP)/Good Manufacturing Practices (cGMP) facility and is registered with the United States Food and Drug Administration (FDA). GLIís FDA registration number is 1020808.
Galbraith is registered with the Consumer Product Safety Commission (CPSC) as an accredited laboratory.
Critical elements of the GMP program include instrument validation, the potential to execute method validation, QA inspection, corrective and preventive actions, software validation, vendor certification, internal audits, and analytical investigations.
GLI is in compliance with the requirements of Code of Federal Regulations (CFR) parts 210 and 211 for analytical subcontract laboratories.