Health Canada Cosmetics Update 2025: What’s Changed and How to Prepare

Canada’s cosmetics regulations are undergoing major changes in 2025, and companies that sell into the Canadian market need to adapt quickly to remain compliant. From new labeling requirements to fragrance allergen disclosures and enhanced safety protocols, Health Canada’s updated rules will impact how products are formulated, packaged, and marketed.  In this webinar, our regulatory expert

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Don’t Become EU Non-Compliant—Understanding the 51st Amendment of IFRA Standards Enforcement on October 30, 2025

Fragrance and flavor ingredients are central to cosmetics and personal care products, but they’re also highly regulated due to their complexity and potential allergens. With the 51st Amendment to the International Fragrance Association (IFRA) Standards going into effect on October 30, 2025, the time to act is now.  This significant update introduces new ingredient restrictions, clarifications, and compliance changes.

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Build Better Cosmetics Faster with Cosmetri: The Ultimate Software Solution for Brand Managers

Join us for a webinar introducing Cosmetri for Brand Managers, the innovative software platform with a focus on the specific needs of brand managers in the beauty and personal care industry. Learn how this all-in-one software will streamline your product development process, manage regulatory compliance, and speed up your product launches.    We will focus

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Adapting to Change: Navigating FDA Regulatory Shifts and Evolving Tariff Policies in 2025

As global trade dynamics continue to shift, customs brokers, international suppliers to the U.S., and importers must stay ahead of critical regulatory and policy changes that directly impact compliance and operations. From the evolving enforcement priorities at the U.S. Food and Drug Administration (FDA) to renewed scrutiny of de minimis thresholds and tariff policy under

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Your roadmap to EU & UK cosmetics compliance: Understanding Regulation (EC) No 1223/2009

In this webinar, we will provide an overview of Regulation (EC) No. 1223/2009, the mandatory regulation required to market cosmetic products in the European Union and the basis for UK Cosmetics Regulation. This regulation ensures that all cosmetic products are safe for consumers, properly labeled, and manufactured under quality standards. Learn how to navigate compliance

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Adverse Events Are Under the Spotlight: What MoCRA Compliance Means for You

This webinar will go into detail about adverse event requirements under the Modernization of Cosmetics Regulations Act (MoCRA) and how important it is for brands and manufacturers to work together to maintain compliance. We will discuss how retailers are aligning with MoCRA’s regulations and asking brands to have a proper system in place to receive,

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Unwrapping FDA’s MoCRA Labeling Regulations

Learn about the labeling requirements mandated by MoCRA as well as the general requirements all cosmetic products must meet. We will describe in detail what must appear on your products’ labels and the timelines for compliance. Topics include:   Meeting the new adverse event contact requirements FDA actions on fragrance allergens Bilingual labeling requirements

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2025 Cosmoprof Bologna

Booth Number: US Pavilion B65 Read more »

New Zealand In-Person Seminar: US FDA Compliance for Cosmetics Products to the USA

The United States regulates the import of all cosmetics, including over-the-counter (OTC) drug products. The agency responsible for enforcing the various requirements is the US Food and Drug Administration (US FDA). The United States recently enacted the Modernization of Cosmetic Regulations Act of 2022 (MoCRA), which significantly expands the regulatory authority of the U.S. Food and Drug

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CARES Act Imposes Fees & Submissions on Drug Industry. Are you Complying?

Since 2020, FDA has imposed more requirements on the drug industry. Besides establishment registrations and product listing that have been required for decades, fees are now collected by the FDA on more manufacturers on an annual basis. Amounts of listed drug products are now required to be reported on an annual basis. Stay out of

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Practical Steps to be MoCRA Compliant Quickly With Cosmoprof

Chiara Remonti, Senior Regulatory Advisor of Registrar Corp will walk you through key provisions of MoCRA, highlighting how they impact your business operations, and what you need to do before Miami. We’ll cover challenges like product listings, navigating FDA’s Cosmetics Direct portal, adverse event reporting requirements, labeling impacts, and more.

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Practical Steps to be MoCRA Compliant Quickly

With the MoCRA regulations now in full effect, staying compliant with the latest US FDA cosmetic industry standards is more crucial than ever. Join us for “Practical Steps to be MoCRA Compliant Quickly,” where we will equip cosmetic brands and manufacturers with the knowledge and strategies needed to navigate the evolving regulatory landscape in 2024

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