Joe Cwiertniewicz is a Quality and Regulatory Compliance Specialist consultant with experience in the FDA and OECD Good Laboratory Practice (GLP), Good Clinical Practices (GCP) and current Good Manufacturing Practices (cGMP) regulations. He has held Director, Quality Assurance, Associate Director of Quality Assurance, Manager of Corporate Compliance, and Senior Compliance Specialist positions with leading pharmaceutical and biotechnology companies. He has experience with computer validation, animal welfare, facility qualifications and licensing issues.  Joe is available to provide support to your quality program on a contract basis.