David Dabbs is equipped with 20+ years of experience managing large validation projects, quality assurance and operation teams in areas of: quality control, regulatory compliance, auditing, and training in the biopharmaceutical industry. Offers proven abilities in defining big-picture vision, quickly analyzing data, leading multi-functional groups, and developing and motivating staff. Additional areas of expertise include:

Equipment Validation • IQ/OQ/PQ ?Total Quality Management • Policy/Procedure Development • Process Improvement ? Inventory and Document Control • Project Management • Auditing • Preventive Medicine

He has also written training programs for the biologics industry and had his training program published in the Plasma Protein Therapeutic Association (PPTA).

He also has 20+ years of experience in assisting companies prepare for FDA pre-licensure and routine inspections to include remediation. Mr. Dabbs also has over 15+ years assisting companies in gaining and maintaining ISO certification and recertification.