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ECHA Refers 2018 REACH Registrants To New Data Search Tools, Funding Options

 
• By Ryan Nelson

The European Chemicals Agency is promoting a searchable list of lead registrants, accessible through a new interactive infographic, among other tools and resources available to support industry compliance, particularly among SMEs, as the 2018 REACH registration deadline draws closer.

The European Chemicals Agency continues work to support pending REACH 2018 registrations amid a building sense of urgency and concerns that many low-volume registrants may be ill-positioned to comply with next year's final phase-in deadline.

The Directors' Contact Group, which facilitates the exchange of views between the European Commission, ECHA and industry associations, issued a...

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More from Regulation

EPR-Impacted Producers: Budget Early, Consider Other State Programs Before Repackaging

 
• By Eileen Francis

Consultants urge packaging producers to forecast and budget now for the fees of state EPR programs, particularly as fees from the Oregon program hit and surprise many firms and expose gaps in internal budgeting and planning. The topic was discussed at IBA’s Cosmetics Convergence 2025 conference.

US FDA’s Delay of Cosmetic GMP Rule, Communication Style Raises Litigation Concerns – Attorneys

 
• By Eileen Francis

The US FDA’s decision to move its long-awaited cosmetic GMPs rule to ‘Long-Term Actions’ under MoCRA likely delays a final rule for at least five years, raising the risk of increased state regulation and private litigation, say attorneys speaking during the 2025 PCPC Science Symposium & Expo

‘You Are Very Regulated’: Consumer Health And Beauty Industries’ Attention Needed In California

 
• By Malcolm Spicer

Regulations likely holding consumer product firms’ attention include the Plastic Pollution Prevention and Packaging Producer Responsibility Act, SB 54, scheduled to become effective by 2027. “Easily the most significant, extended producer responsibility law ever to pass in the world,” says lobbyist

US FDA Independence Questioned At CDC Oversight Hearing

 
• By Michael McCaughan

A Senate committee is investigating leadership changes at the US Centers for Disease Control and Prevention. While the primary focus is vaccine policy, the first hearing suggested the probe could raise questions about FDA independence.

More from Policy & Regulation

US FDA’s Delay of Cosmetic GMP Rule, Communication Style Raises Litigation Concerns – Attorneys

 
• By Eileen Francis

The US FDA’s decision to move its long-awaited cosmetic GMPs rule to ‘Long-Term Actions’ under MoCRA likely delays a final rule for at least five years, raising the risk of increased state regulation and private litigation, say attorneys speaking during the 2025 PCPC Science Symposium & Expo

Industry Should Assume More Holistic, Integrated Approach To Animal Alternative Tests

 
• By Eileen Francis

Scientists at a session of the 2025 Personal Care Products Council’s Science Symposium & Expo on Oct. 28 emphasized that new approach methodologies for chemical safety testing should move beyond simple one-to-one animal test replacements toward integrated, holistic strategies.

FDA Position On Animal Alternative Sunscreen Tests Reflects ‘Troubling Disconnect’ – PETA

 
• By Lauren Nardella

The US Food and Drug Administration is advocating for the development of new alternative methods while specifying that animal tests are needed for sunscreen UV filters, creating uncertainty about the future of NAMs, say animal rights and industry groups.