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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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The FDA’s Modernization of Cosmetics Regulation Act introduces new requirements for the cosmetics industry, significantly increasing regulation for the first time since 1938. Key changes include: Facility Registration: Companies must register their manufacturing facilities with the FDA. Product Listings: All marketed cosmetic products, including their ingredients, must be listed and updated with the FDA. Adverse

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

Registrar Corp Launches Adverse Events Management Software for FDA MoCRA Compliance Hampton, Va., July 23, 2024 — Registrar Corp, the world’s largest FDA compliance company with 32,000 clients in 190 countries, announced today the launch of Adverse Event Management (AEM) Software.  The first-of-its-kind software enables cosmetics companies to comply with the U.S. Food and Drug Administration’s (FDA) Modernization

July 23, 2024, Registrar Corp (“Registrar”), a Paine Schwartz Partners portfolio company and the U.S.’ leading provider of regulatory and compliance software for food, cosmetic, and life science companies, has acquired Foodsteps, a pioneering UK-based company dedicated to helping food businesses reduce the environmental impact of their products.  Foodsteps was launched in 2018 by Cambridge University

HAMPTON, Va., May 8, 2024 /CISION/ — Registrar Corp, the leader in U.S. Food and Drug Administration (FDA) registration and compliance, proudly announces its achievement of the prestigious ISO 27001 certification, marking a significant milestone in the company’s ongoing commitment to data security and protection. Serving over 30,000 companies across more than 190 countries, Registrar

New FSVP compliance software ComplyHub helps U.S. food importers monitor suppliers, manage documents, and boost business growth.

World’s largest FDA compliance company is ready on day one, already serving the needs of hundreds.  Click to read the original release.  HAMPTON, VA, Month Day, 2023 (Distributor) — Registrar Corp, the leading regulatory compliance services, training, and software firm for all things FDA has begun leveraging its extensive Structured Product Labeling (SPL) expertise to

World’s Largest FDA Compliance Software Firm Positioned to Meet Demand from New Cosmetics Industry Regulation with Expanded Capabilities.

New Adverse Event Reporting software and services help save cosmetic companies time and effort in complying with updated FDA regulations.

Introducing MoCRA Wizard, the newest tool from Registrar Corp to quickly understand your responsibilities under MoCRA

Read this press release on PRNewswire. Hampton, Virginia, July 12, 2023 – Registrar Corp, the leading compliance services, training, and software firm, is pleased to announce a new partnership with the Independent Beauty Association (IBA), a nonprofit trade organization that represents independent beauty brands and companies.  This strategic partnership brings together Registrar Corp’s expertise in