Labeling Guidance Asks For Too Much Detail On Dosage & Administration – PhRMA
Executive Summary
The amount of information to be included in the Dosage and Administration section of labeling under a recent draft guidance may be too detailed for certain drug products, the Pharmaceutical Research and Manufacturers of America say in comments submitted on the draft
You may also be interested in...
Draft Guidance Explains Inclusion Of Pharmacologic Class In New Labeling
FDA's standards for an "established" pharmacologic class are that the agency has determined the class is both scientifically valid and clinically meaningful, according to a draft guidance released May 15
IFRA Hosts Capitol Hill Scent Experience In Timeout From Policy Concerns
The International Fragrance Association North America took a break from its higher-stakes advocacy work Nov. 1 to give lawmakers and congressional staffers a "scent experience." Perfumers from six of the group's biggest members were on hand with "Scents of Home," joined by Monell Center researchers to educate attendees on the mechanics of scent and the important role it plays in people's lives.
NSF's Cosmetics Verification Program Fizzles, While EWG's Could See Second Boom
NSF International has put its cosmetic product verification program on ice due to lack of interest since its launch in April 2017. Meanwhile, more than 1,000 products from 75+ brands have earned the "EWG Verified" mark, and the NGO says interest is higher than ever following Walmart's announcement in September that it will begin pushing vendors to pursue the verification.