Ms. Christina Fair has more than a decade of experience in the health industry with over six years of management experience. Christina has worked in all areas of GMP compliance and has developed and implemented quality management systems and improvements of pre-existing quality systems. During her tenure in industry, she worked in several quality assurance roles and developed expertise in several areas, including: writing, reviewing, and approving SOP's, batch records, technical reports, validation protocols, validation master plans, training material, CMC submissions and drug master files. She also trained personnel on cGMPs, equipment, software, purification and analytical methods. Christina participated in external audits (clients, investors and FDA), and also PAIs. Christina also has experience speaking to the FDA one-on-one as the corporate representative.