Third-Party Dietary Supplement AER Oversight Supported By Industry
This article was originally published in The Tan Sheet
Executive Summary
Dietary supplement adverse event reports could be collected by a scientific institution in a way that would enable all interested parties to review the data and collectively determine how to act on them, attendees at a May 8 Supply Side East symposium in Secaucus, N.J. agreed.
You may also be interested in...
Voluntary AE Anonymous Database Targeted For Ingredient Surveillance
The American Herbal Products Association will seek FDA input on a proposed, industry-sponsored dietary supplements adverse event system through which participating companies would submit all AE reports to an anonymous database reviewable by the agency.
Voluntary AE Anonymous Database Targeted For Ingredient Surveillance
The American Herbal Products Association will seek FDA input on a proposed, industry-sponsored dietary supplements adverse event system through which participating companies would submit all AE reports to an anonymous database reviewable by the agency.
Voluntary AE Anonymous Database Targeted For Ingredient Surveillance
The American Herbal Products Association will seek FDA input on a proposed, industry-sponsored dietary supplements adverse event system through which participating companies would submit all AE reports to an anonymous database reviewable by the agency.