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Adverse Event Reporting for OTC Drug Products

Adverse Event Reporting for OTC Drug Products

By EAS Senior Advisor for OTC Drugs and Labeling Susan Crane The Food and Drug Administration monitors the safety of drug products marketed in the United and requires the pharmaceutical industry to document and, as applicable, report adverse events experienced by...

Crane Return to CHPA OTC 101 Academy

Susan Crane, Independent Advisor for OTC Drugs and Listings is an invited speaker at the CHPA OTC Academy and Workshop taking place in Wilmington, DE October 28-29, 2019. OTC Academy is a great learning opportunity for those new to the industry and those wishing to...

OTC Monograph System Gets an Update

By Susan Crane This month’s Ask the Expert is answered by EAS Independent Advisor for OTC Drugs and Labeling, Susan Crane. Susan specializes in quality and regulatory compliance for over-the-counter (OTC) and dietary supplement products. She has a thorough knowledge...