Medtech Insight is part 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

Supplement adverse event reporting overseas suggested as U.S. model -- Farnsworth.

This article was originally published in The Tan Sheet

Executive Summary

SUPPLEMENT COMMISSION CONSIDERS MANDATORY ADVERSE EVENT REPORTING SYSTEM to collect data on dietary supplement safety. At the President's Commission on Dietary Supplement Labels Oct. 24 meeting in Washington, D.C., Chair Malden Nesheim, PhD, Cornell University, said the group is leading up to "the potential recommendation" that there needs to be an obligatory adverse event reporting system for dietary supplement marketers.

Topics

UsernamePublicRestriction

Register

PS086276

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