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New in Regulatory (page 12 of 20)
Jun 02, 2008 | 05:10 PM CDT
The European Chemicals Agency (ECHA) has published two new guidance documents.
May 14, 2008 | 04:07 PM CDT
By: Jack Corley, Trilogy Fragrances Inc.
The growth in natural and organic personal care products has resulted in a need for logical, practical and achievable standards. Conventional wisdom would tell us that the name of a product and the ingredients used to make that product are meaningful and truthful as reflected on the product label. But the fact is labeling cosmetics often depends entirely on the manufacturer.
May 14, 2008 | 03:36 PM CDT
By: Jeb Gleason-Allured, Editor
Protecting formulas, sources and other forms of intellectual property in a thriving regulatory environment. The Fragrance Materials Association (FMA; fmafragrance.org) and Flavor and Extract Manufacturers Association (FEMA; femaflavor.org) recently co-hosted an in-depth webinar on key intellectual property (IP) issues, particularly the protection of formulas when faced with disclosure requests from customers, physicians, the public and other sources.
May 14, 2008 | 10:08 AM CDT
Last October 2007, California Assemblywoman Fiona Ma introduced legislation to ban the use of phthalates in California. The law was passed by the California Legislature and will take effect in January 2009.
May 14, 2008 | 09:59 AM CDT
The European Chemicals Agency (ECHA) has announced it will conduct a completeness check of registration dossiers under REACH within three weeks of their submission.
May 14, 2008 | 09:47 AM CDT
Legislation that would emphasize the need for federal agencies to address environmental, health and safety questions concerning nanotechnology was approved by the House Science Committee on May 7, 2008.
May 12, 2008 | 10:58 AM CDT
A new label takes on the unregulated arena of organic personal care
May 06, 2008 | 09:54 AM CDT
Gay Timmons (Oh, Oh Organics) explains the needs for organic production and certification at the Oasis introductory event at Natural Products Expo West.
Apr 25, 2008 | 01:37 PM CDT
The European Commission has adopted a regulation for the fee schedule for registration under REACH.
Apr 25, 2008 | 12:48 PM CDT
The US House Committee on Energy and Commerce recently released a draft of legislation, The Food and Drug Administration Globalization Act of 2008, which is intended to stimulate discussion about how to provide adequate funding and authority for the FDA to ensure the safety of the nation's food, drug, medical device and cosmetic supply in an increasingly globalized marketplace.