Regulatory

Whitehouse Laboratories is

  • cGMP-compliant,
  • FDA established,
  • DEA (Schedules II through V) registered,
  • ISO 17025 certified and
  • ISTA certified (Member ID:  ST-10055).

Whitehouse Laboratories has been audited and inspected by the FDA various times throughout its existence and currently maintains a no Form 483 status. We are committed to strict cGMP quality standards and we adhere to a multiple level internal data review process to ensure the accuracy and integrity of each test assignment we undertake.

Most Recent FDA Inspection Results

Date of Inspection: March 2015

No 483 Issued

No Observations Noted

Date of Inspection: September 2012

No 483 Issued

No Observations Noted

Date of Inspection: July 2009

No 483 Issued

No Observations Noted

Date of Inspection: December 2006

No 483 Issued

Index of Licenses, Certifications and Registrations

  • US Food & Drug Administration – Registration of Drug Establishment  (FDA)

  • Federal Drug Enforcement Agency Registration Certificate (Form 225)

  • New Jersey State Department of Health – Controlled Dangerous Substances Schedules II-V

  • Environmental Protection Agency – Hazard Waste Disposal

Christine Paisker
Quality Assurance Manager
Direct: 908-823-9300
Christine.Paisker@amriglobal.com