Lachman Consultant Services
Kris Durst holds a Master of Science in Quality Assurance/Regulatory Affairs from Temple University. With a background in Chemical Engineering and Chemistry from West Virginia University, Kris has extensive experience in the pharmaceutical and biotech industry. As the Owner and Principal Consultant of GxP Consulting Services, Kris provides a range of services including FDA response assistance, validation documentation, and SOP review. Additionally, as a Senior Associate at Lachman Consultant Services and Senior Quality Consultant at Parexel, Kris has been involved in various audit, remediation, and quality support projects. Kris has also worked as a Principal Consultant at NSF International, focusing on ANDA analytical method validation. With a career spanning over two decades, Kris has demonstrated expertise in quality management, validation engineering, and regulatory compliance across multiple organizations.
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Lachman Consultant Services
Experience. Excellence. Founded in 1978, Lachman Consultants serves companies in Pharmaceutical, Medical Device/Combination Products, Biologics, and Regulatory Affairs. Each practice offers industry-leading experience and expertise in its area of focus. Lachman Consultants serves emerging-to-enterprise organizations on a worldwide basis, delivering solutions that include FDA-Related Services, Audits & Mock Inspections, Quality Assurance & Controls, Scientific and Technical Assistance, Systems Evaluation, Regulatory Affairs, and Training, which consistently exceed client requirements and expectations. When it comes to compliance and regulatory affairs, Lachman has set the industry standard through senior consultants, efficient engagements, integrated expertise, and loyal clients.