Analytical Lab Group is a group of EPA established and FDA-regulated contract testing laboratories that function as an extension of our clients’ quality management systems. We have developed and implemented a quality management system that enhances our ability to provide testing services that consistently meet client expectations and regulatory requirements. The quality management system also ensures that ALG avoids involvement in any activities that would diminish confidence in its competence, impartiality, judgement or operational integrity.
The ALG quality documentation requirements are defined by the following:
EPA 40 CFR Part 160 FIFRA Good Laboratory Practice Standards
FDA 21 CFR Part 58 Good Laboratory Practice For Non-Clinical Laboratory Studies
FDA 21 CFR Part 210 Current Good Manufacturing Practice in Manufacturing, Processing, Packing or Holding of Drugs; General
FDA 21 CFR Part 211 Current Good Manufacturing Practice for Finished Pharmaceuticals
FDA 21 CFR Part 11 Electronic Records, Electronic Signatures – Scope and Application
ISO/IEC 17025:2017 General Requirements for the Competence of Testing and Calibration Laboratories
Contact Us to request specific information about our company and quality management system.