Meredith L. Crabtree is a Regulatory Compliance and Quality Systems expert with over 30 years of hands-on experience in FDA-regulated industries, including pharmaceuticals, medical devices, biologics, dietary supplements, cosmetics, and animal health products. She specializes in quality system development, regulatory strategy, auditing, and training, helping organizations navigate complex FDA, DEA, and ISO requirements. Meredith provides consulting services across life science industries, supporting clients with FDA inspection readiness, supplier audits, deviation management, CAPA programs, labeling compliance, and regulatory submissions. She is known for her practical, risk-based approach to quality management and her engaging, real-world training style. In addition to her consulting practice, Meredith serves as an accreditation inspector for the American Association of Tissue Banks (AATB) and is a frequent presenter on regulatory compliance topics.