Frank Verni, R.Ph., MPH joined the FDA in 2007 as an Investigator in the Office of Regulatory Affair’s (ORA’s) New York District. Frank conducted numerous inspections and investigations at pharmaceutical, medical device and dietary supplement firms. Frank later became a compliance officer within ORA’s New York District where he was responsible for the review of all pharmaceutical cases within his region. Currently, Frank is working as a Compliance Officer in CDER’s Office of Compliance in the sub Office of Manufacturing Quality. Frank is responsible for the review of both foreign and domestic pharmaceutical inspections for deficiencies that may potentially warrant advisory and enforcement actions by the FDA in order to protect patients from firms whose quality standards and practices may pose a significant risk to public health. Prior to the FDA, Frank was a clinical and compounding pharmacist in the New York metro area.