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Tackling Environmental Science Issues
The Industry continues to push before the Food and Drug Administration (FDA) predictable policies and timelines in household regulations.
In February 2020, during a CLP dialogue with Sen. Koko Pimentel the FDA committed to fast-track the process with the caveat that registrants must submit complete documents. After that dialogue, speed in the processing was achieved. To further achieve a common undertaking of GHS compliance, CLP sponsored a webinar on GHS Bridging Principles. One notable gain of CLP’s advocacy with FDA is the decrease in quantity of Amount of Reference Standards from 1 gram to 250 milligrams, a request that FDA granted |
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