Steve Nava
Quality Assurance and Regulatory Affairs
Quality Assurance / Regulatory Affairs Professional with 16+ years of experience in the development, implementation and adherence of regulatory policy within the bio-pharmaceutical industry, with emphasis on Chemistry, Manufacturing, and Controls (CMC). Skilled in cultivating highly effective partnerships with global health authorities, in concert with CROs, as well as the FDA to facilitate drug development activities. Exceptional leadership, communication and negotiation skills. ISO9000 Trained Auditor with solid foundation in worldwide quality and regulatory requirements and thorough knowledge of cGMPs, GCPs, and GLPs guidelines. BS in Chemistry and Mathematics.
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