Oxford Pharmaceutical Resources

Oxford Pharmaceutical Resources, Inc. is a specialized consulting clinical and regulatory organization (CRO) based in Totowa, New Jersey. Founded and led by Dr. Richard A. Guarino, a renowned expert in the drug approval process and author of the 'New Drug Approval Process' textbook, the firm provides strategic guidance to pharmaceutical and biotechnology companies. Their core services include the planning, implementation, and submission of Investigational New Drug (IND) and New Drug Applications (NDA) in the Common Technical Document (CTD) format. The company also offers expertise in Good Clinical Practice (GCP) training, clinical trial protocol design, and FDA liaison services to facilitate the efficient development and approval of new therapeutic products.