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Adverse Events, Serious or Not?

By Norma Skolnik This month’s Ask the Expert question on Serious Adverse Events Reporting is answered by Independent Consultant, Norma Skolnik. Norma has over 35 years of regulatory experience working with the pharmaceutical, OTC drug, and dietary supplement...

Does Our Company Offer Enough Training?

By Karen Dixon EAS is pleased to introduce a new column in our EAS-e-News called Ask the Expert. Each month our expert consultants and Senior Directors will answer one question sent in by readers (edited if applicable to remove identifying information). If you’d like...

Ask the Expert January 2018

By Allen Sayler EAS Webinar on FDA Draft Guidance: “Control of Listeria monocytogenes in Ready-To-Eat Foods: Guidance for Industry” October 31, 2017 EAS received an overwhelming response to our recent webinar on controlling Listeria monocytogenes in ready-to-eat...