Paula Simone

Paula Simone is a Senior Regulatory Submissions Manager with over 20 years of experience in Regulatory Operations and Project Management. Paula has previously worked at various pharmaceutical companies, including Actavis (now Allergan), where they provided critical support to the Regulatory Affairs department and managed the preparation of submissions to the FDA. At Teva Pharmaceuticals, Paula led the publishing of regulatory documents, ensuring compliance for INDs, NDAs, and ANDAs. Currently, Paula is pursuing a Master’s in Health Auditing Specialization and a Bachelor’s in Psychology from Universidad Autonoma de Manizales and Universidad de Manizales, respectively.