Quality

Advanced Analytical Testing Laboratories operation has a formal quality assurance program adhering to guidelines of current Good Manufacturing Practices (cGMP) 21 CFR part 210, 211 and 820 of the US Food & Drug Administration (FDA).

Quality Assurance Procedures are strictly adhered to and followed by all laboratory personnel including executive management, lab administrators, managers, scientists and consultants.

The QA group routinely audits procedures and practices governing facilities, equipment, maintenance, instrument calibration, general lab procedures, client specific testing procedures, data reporting and data archiving.