Robert Zeid
Senior Associate, Regulatory Affairs
Expert in regulatory documentation and submissionBob Zeid is an international regulatory affairs expert who provides medical/ technical writing services for drug and biologics product submissions. He provides regulatory and product liability support for US and international regulatory filings. He performs GLP, cGMP, and mock PAI inspections. As a certified trainer for controlled substances (CS) compliance, he provides training programs and CS audits.
Prior to working with PharmaDirections, Mr. Zeid was a Senior Regulatory Associate at AAI and at Univax Biologics His special expertise includes writing and reviewing chemistry, manufacturing, and control (CMC) documents for regulatory submissions, preparing documents for meetings with the FDA or other competent authorities, regulatory & cGMP training, design, and implementation of environmental monitoring (EM) systems and overall GMP compliance.