Lead the Regulatory and Quality Compliance department, directs programs, policies and practices to ensure business practices are in compliance with FDA, Good Clinical Practices (GCP) and Good Laboratory Practices (GLP) and Good Research Practices (GRP). Responsible for the definition and development of standards for company-wide compliance with all applicable Federal, state and local regulations. Reviews and evaluates compliance issues/concerns within the organization. Represents organization with regulatory bodies and agencies
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