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The federal government has introduced new regulations to improve the safety of cosmetic products, marking the most significant FDA updates on cosmetics in 85 years. These changes focus on three key areas: professional-use products, adverse event reporting labels, and fragrance allergen labeling. First, makeup products intended for professional use now require clear labeling to indicate

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New requirements from the FDA could impact your medicine cabinet, your shower routine and even your skin. The rules will change the way cosmetic brands do business. Registrar Corp cofounder and president David Lennarz calls them a long time coming. “There’s only been voluntary requirements for the cosmetics industry essentially since the Food Drug and

New scrutiny from the U.S. Food and Drug Administration (FDA) aims to make cosmetics safer, officials said. On July 1, companies that make products like makeup, shampoo, skincare, artificial eyelashes, tattoo ink, mouthwash, hair dyes, sunless tanning lotions, and waxing kits began adhering to strict FDA regulations, the first of which in over 85 years.

Registrar Corp. has introduced an Adverse Event Management (AEM) software in response to the FDA’s Modernization of Cosmetics Regulation Act (MoCRA). This new regulation mandates that cosmetic brands include contact information on both primary and secondary packaging for reporting adverse events. The software provides companies with a brand-specific URL or QR code, enabling consumers to

The article focuses on the impact of the Modernization of Cosmetics Regulation Act (MoCRA) on the cosmetics industry, emphasizing the shift toward improved adverse event reporting and our new AEM Software. The new regulation, which came into effect at the end of 2023, requires cosmetic companies to enhance transparency by listing contact information on packaging

Introducing AEM, (Adverse Event Management software), a first-of-its-kind platform designed to help cosmetics companies comply with the FDA’s Modernization of Cosmetics Regulation Act (MoCRA). The software securely collects sensitive data, tracks adverse events globally, and formats serious cases for FDA submission in the MedWatch format. MoCRA’s complex reporting requires coordination across various departments, including compliance,

Registrar Corp has introduced its Adverse Event Management (AEM) software to aid the cosmetic industry in complying with the FDA’s Modernization of Cosmetics Regulation Act (MoCRA). MoCRA introduces stricter requirements for cosmetic product safety, including displaying contact information on packaging, collecting consumer medical data, and reporting serious adverse events to the FDA within 15 days.

Registrar Corp has launched its Adverse Event Management (AEM) software to assist cosmetics companies in meeting the FDA’s new requirements MoCRA mandates. These mandates include displaying contact information on packaging, collecting detailed consumer medical data, investigating adverse events, reporting serious cases to the FDA within 15 days, and maintaining records for up to six years.

Registrar Corp, the largest FDA compliance company, has introduced Adverse Event Management software tailored to help cosmetics companies meet new requirements under the FDA’s Modernization of Cosmetics Regulation Act (MoCRA). MoCRA sets stringent rules for reporting adverse events, including displaying contact information on packaging, collecting consumer medical data, and submitting serious event reports to the

Under MoCRA, federal government has introduced new safety regulations for cosmetic labels, representing the most significant FDA updates in 85 years. These changes focus on three main aspects: professional-use makeup, complaint reporting labels, and fragrance allergen labeling. First, cosmetics designed for professional use must now have a clear label stating they are not intended for

The federal government has rolled out new MoCRA requirements aimed at improving cosmetic safety, marking the most substantial FDA changes to cosmetic legislation  in 85 years. These updates focus on three critical areas: labeling for professional-use products reporting adverse events identifying fragrance allergens To begin with, products intended for professional use now require a distinct

The FDA has introduced new MoCRA rules that will affect various aspects of cosmetics, including those found in your medicine cabinet, shower routine, and skincare products. These rules represent a significant shift for cosmetic companies, who will now have to comply with more stringent requirements. According to David Lennarz, co-founder and president of Registrar Corp.,

In this video, Jaclyn Bellomo, Director of Cosmetic Science and Regulatory Affairs at Registrar Corp., discusses the significant changes introduced by the Modernization of Cosmetics Regulation Act (MoCRA). As the most extensive update to cosmetics regulations in over 80 years, MoCRA brings new requirements aimed at enhancing consumer safety and increasing transparency within the cosmetics

In this video, David Lennarz, President of Business Development and Operations at Registrar Corp., discusses the FDA’s new MoCRA adverse event regulations. The updated rules aim to enhance consumer safety and transparency in the cosmetics industry. Lennarz explains that cosmetics labels must now include information for reporting adverse events, such as skin reactions. Brands are