FDAQRC offers specialized quality consulting, regulatory compliance and quality assurance for Pharmaceutical, Medical Device and Biotech companies. We provide customized, value-added solutions, processes and enhanced quality standards to optimize business efficiencies and minimize regulatory risk.
We do more than audits; we collaborate with you to analyze your need and match the right expert to your situation.
Our global team is recognized as experts in quality assurance and regulatory affairs providing expert advice to pharmaceutical, medical device and contract research organizations in pre-clinical, clinical and commercialized sectors.
Industry
Pharmaceutical Manufacturing
HQ Location
100 E. Whitestone Blvd
Suite 148-262
Cedar Park, Texas 78613, US
Keywords
Quality System ImplementatioGap Analysis AuditsGood Clinical Practice AuditsRisk AnalysisDue Diligence auditsGood Manufacturing Practice audits (Pharma/Medical Device)RemediatioLiterature Review 505(b)(2)Good Laboratory Practice AuditsPharmacovigilance