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Tamika Cathey

Global Principal Technical Lead, Pharma Biotech Dietary Supplement Consulting & Life Sciences
Life Sciences

Tamika Cathey has over 20 years of experience in regulatory enforcement, regulatory compliance and quality management. As an industry consultant, she works with organisations across industries, including pharmaceuticals, Active Pharmaceutical Ingredients (APIs), dietary supplements, biologics, tobacco, and medical devices.

Prior to NSF, she served as the Consumer Safety Officer at the US Food & Drug Administration (FDA), working in regulatory inspections, FDA compliance, CAPA remediation and enforcement actions under FDA 483s, including warning letters and consent decrees.

Tamika holds a Bachelor of Biological Science from Greensboro College.

Her areas of expertise include:

  • Inspection readiness.
  • cGMP and GCP auditing.
  • Lead auditor and risk management training.
  • Strategic planning and gap assessments.
  • FDA 483s, warning letters and consent decrees removal.