Allen Fields is responsible for Clinical Affairs, Customer Service and REMS, Drug Safety/Pharmacovigilance, Pharmaceutical Development, Project Management, Regulatory Affairs, and Research and Development.
Allen has more than 30 years of experience as a clinical and regulatory affairs professional. He has managed IDEs, INDs, MAAs, NDAs, BLAs, ANDAs, SNDAs, 510Ks and PMAs. He has led drug development programs, due diligence, preparation of documents, strategic clinical and regulatory planning, and has had meetings with the global regulatory agencies. His expertise in drug development in all phases of development has led to over 40 approvals. He has held senior clinical and regulatory affairs positions at small and large pharmaceutical firms, including Oread, TAP Holdings, Purdue Pharma, Alliant Pharmaceuticals, and Quintiles International.
Allen holds a B.S. in Chemistry from Kansas Wesleyan University; M.Ed./M.S. work at Kansas State University; graduate work at University of Kansas School of Medicine; Neuropharmacology Fellowship; and additional graduate work at Duke, Johns Hopkins, and Walden University.