Dr. Moffett has been with Nuventra since 2016 with a primary focus on Regulatory Affairs, Regulatory Operations, and Project Management. Dr. Moffett is the lead publisher for eCTD submissions within Nuventra and has been directly involved with the preparation of eCTD submissions for both IND and marketing applications to the FDA. In addition, Dr. Moffett has experience in authoring nonclinical and clinical modules of regulatory submissions as well as a diverse array of other regulatory and scientific documents.
Education