Harman Dubé has been appointed vice president of the Preclinical and Regulatory Affairs group within OckhamCRO. Dr. Dubé has 14 years of experience in developing and directing a variety of drug and device development programs, supporting pharma and biopharma organizations with development efforts. Her areas of experience include consultation on, and management of, non-clinical studies, CMC activities and U.S. and International regulatory filings, technical writing and project management. Pri...