Pink Sheet is part of the Business Intelligence Division of Informa PLC

This site is operated by a business or businesses owned by Informa PLC and all copyright resides with them. Informa PLC’s registered office is 5 Howick Place, London SW1P 1WG. Registered in England and Wales. Number 8860726.

This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

Printed By

UsernamePublicRestriction
UsernamePublicRestriction

Adverse Event Screening System Under Development At U. Of Minn.

This article was originally published in The Tan Sheet

Executive Summary

A national adverse event report database would be used to cull serious events from all AE data before submission to FDA, according to a proposal being considered by the dietary supplement and OTC drug industries
Advertisement

Related Content

Minnesota Supplement Safety Center Vies For Congress’ Ear
Minnesota Supplement Safety Center Vies For Congress’ Ear
Minnesota Supplement Safety Center Vies For Congress’ Ear
Senators Durbin, Hatch To Work Together On AER Plan
Senators Durbin, Hatch To Work Together On AER Plan

Topics

Advertisement
UsernamePublicRestriction

Register

PS097002

Ask The Analyst

Please Note: You can also Click below Link for Ask the Analyst
Ask The Analyst

Your question has been successfully sent to the email address below and we will get back as soon as possible. my@email.address.

All fields are required.

Please make sure all fields are completed.

Please make sure you have filled out all fields

Please make sure you have filled out all fields

Please enter a valid e-mail address

Please enter a valid Phone Number

Ask your question to our analysts

Cancel