Rigorous Quality Assurance

The Whitehouse Lab team  operates a formal quality assurance program adhering to guidelines of current Good Manufacturing Practices (GMP) of the US Food & Drug Administration (FDA).

Quality Assurance (QA) responsibilities are shared by all laboratory personnel including executive management, lab administrators, managers, scientists and special consultants. The QA group routinely audits procedures and practices governing facilities, equipment, maintenance, instrument calibration, general lab procedures, specific testing procedures, data reporting and data archiving.

Standard Operating Procedures (SOP's) are updated according to a strict schedule or as required by the introduction of new methodologies. Standard reference and proficiency tests are used, where applicable, to insure accuracy and precision of all analytical procedures.

Regulatory agencies inspect the laboratory periodically during unscheduled performance investigations. The most recent FDA inspection occurred July 30th to August 5th 2009. The results of this inspection: NO 483 Issued, No Observations Reported.

The Lab's management team maintains an open-door policy. Current and prospective clients are encouraged to visit the facility at any time. Formal qualification audits may be scheduled through the Quality Assurance Manager.

The following regulatory registrations are held by Whitehouse Labs:

• United States Food and Drug Administration
• Federal Drug Enforcement Agency (Schedules 2-6)
• NJ State - Controlled Dangerous Substances
  
• Environmental Protection Agency - Hazard Waste

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