Cosmetic Good Manufacturing Practice Regulation Audits

EAS has former FDA investigators, laboratory personnel, and industry quality experts available to conduct GMP/Quality Systems audits of your suppliers, contract manufacturing and laboratory facilities to assess compliance with applicable FDA and state regulatory requirements as well as established best practices. Our assessments are thorough and complete. You will receive a detailed report outlining your current level of compliance against the Draft Guidance for Industry: Cosmetic Good Manufacturing Practices, with our recommendation as to what needs to be done to bring identified deficiencies into compliance.