Pink Sheet is part of Pharma Intelligence UK Limited

This site is operated by Pharma Intelligence UK Limited, a company registered in England and Wales with company number 13787459 whose registered office is 5 Howick Place, London SW1P 1WG. The Pharma Intelligence group is owned by Caerus Topco S.à r.l. and all copyright resides with the group.

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

SIDI could be useful for NDIs

This article was originally published in The Tan Sheet

Executive Summary

FDA expects the Standardized Information on Dietary Ingredients program to be a "valuable tool" for collecting new dietary ingredient notification information, Council for Responsible Nutrition VP for Scientific and Regulatory Affairs Andrew Shao tells supplement industry executives at CRN's annual conference Oct. 4. FDA's Center for Food Safety and Applied Nutrition director of dietary supplement programs, Bill Frankos, told CRN it provides the "same type of information that FDA looks for in those notifications that they never get." In his presentation, Shao provided an overview of SIDI, a voluntary program established by supplement industry trade groups in October 2006 to simplify and standardize the exchange of information between ingredient suppliers and product manufacturers (1"The Tan Sheet" Oct. 23, 2006, p. 8). CFSAN Director Robert E. Brackett stated NDIs marketed without undergoing the NDI notification process is one of the agency's top concerns...

You may also be interested in...



SIDI Program Will Standardize Ingredient Protocol – Supplement Trade Groups

A voluntary protocol could prompt "a major paradigm shift for many in the [dietary supplement] industry by moving away from unique individualized questionnaires towards standardized documentation and information exchange," trade groups say

Keeping Track: Cancer Approvals From Lumisight Imaging To Adjuvant Alecensa

The US FDA’s approval of Lumicell’s optical imaging agent Lumisight makes a dozen novel approvals in 2024 for the Center for Drug Evaluation and Research.

Partisan Politics Returns To US FDA Congressional Oversight

The US FDA has stood out as an agency that tends to draw broad bipartisan support amid a generally rancorous and divided Congress. A House hearing, however, may be a sign that those days are over.

Topics

Latest Headlines
See All
UsernamePublicRestriction

Register

PS101007

Ask The Analyst

Ask the Analyst is free for subscribers.  Submit your question and one of our analysts will be in touch.

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