Want to be a hands on contributor and responsible for the new drug application process? Keep reading now...What Regulatory Affairs and Product Development contributes to Cardinal HealthRegulatory Affairs & Product Development is responsible for clinical development, nonclinical development, and regulatory affairs consulting to provide innovative solutions and regulatory submissions for all aspects of pharmaceutical, biologics and device development from discovery through post-approval maintenance. Roles and ResponsibilitiesAuthorship and/or review and oversight of creation of eCTDs for drug submission to US and outside-US Health AuthoritiesSupport regulatory strategy for drug developmentEnsu