Data Integrity SME
Indianapolis Indiana USA
Orlando has worldwide pharmaceutical experience with relevant work in computer systems regulatory requirements including US, EMA, Australian, Japanese, WHO, PIC/S, and ICH regulations and guidance's.
Experience with direct participation in FDA agency remedial action plans, regulatory inspections, response activities, and consent decree remediation related verifications.
He is s member of the Pharmaceutical Engineering Editorial Review Board.
Jan 15, 2004