ROSS LOBELL, PH.D.

Regulatory  Affairs  Lead  

Ross is currently the Vice President of Regulatory Affairs for Regsource Consulting, a company dedicated to providing expertise in all areas of drug development. Ross is a seasoned regulatory professional with over 30 years of experience in biopharmaceutical drug development gained across several multi-national, multi-billion dollar companies, including Schering-Plough, Pfizer, Amgen and Astra-Zeneca/MedImmune. Ross has participated in all aspects of the drug  development process, from hands on tactical support to leadership roles across a variety of  small molecule and biologic products. Ross has led the development, submission and review  management process for 2 original NDAs, and 3 original BLAs (one of which included a diagnostic test), 4 of which were approved on the first review cycle.

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