The EUDAMED Deadline Is Approaching: What Manufacturers Must Do Now

As the European Union moves toward full EUDAMED implementation, medical device manufacturers face a critical shift from regulatory awareness to operational execution. With key deadlines in May 2026 for new devices and November 2026 for legacy devices, organizations must ensure their data, systems, and processes are fully aligned to meet compliance requirements before market access is impacted. 

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The Role of Labeling & Regulatory Requirements in OTC Monograph Launch Strategy

Discover what it takes to confidently market OTC drug products in today’s evolving regulatory landscape.    In this in-depth webinar, we’ll break down the fundamentals of FDA OTC drug compliance—starting with how to determine whether your product qualifies as a cosmetic, a drug, or both. From there, we’ll guide you through the essential components of a

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Cosmetics in 2026: Critical EU & UK Regulatory Changes Every Brand Must Prepare For

Regulators in the EU and UK are introducing significant cosmetic regulatory updates that will directly impact ingredient selection, labeling, safety assessments, and product claims.     Many brands are underestimating the scope — and the timeline.     Expanded fragrance allergen disclosures will require label updates. New CMR classifications may trigger reformulation. Silicone and nano ingredient changes could affect

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Unlocking the U.S. Food Market: FDA Regulations that Govern Exports to the USA

Join Registrar Corp and the U.S. Commercial Service of the U.S. Embassy in Singapore for an exclusive webinar tailored for food and beverage exporters across ASEAN looking to enter and succeed in the U.S. market.     This webinar, “Unlocking the U.S. Food Market: FDA Regulations that Govern Exports to the USA,” will feature expert insights from

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Cosmetics Labeling Requirements Across Major Markets

Expanding into global markets brings exciting opportunities—but it also introduces complex labeling challenges. This session provides a clear, side-by-side comparison of labeling requirements in the United States, Canada, the European Union, and the United Kingdom, helping brands prevent costly mistakes and streamline packaging across regions.  Attendees will learn the essential rules that govern cosmetic and

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From Rejection to Approval: China Manufacturer’s Guide to Global Success

Join us for this informative webinar designed for China-based pharmaceutical and API manufacturers preparing Master File (MF) submissions to global regulatory agencies, including the U.S. FDA, Health Canada, EMA, and others. This session will provide essential insights into the MF lifecycle and help ensure your submissions are secure, complete, and compliant.  Topics include:  Types of

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Unpacking U.S. FDA Food Labeling and Ingredient Regulation: What Companies Must Know Before Exporting 

Did you know that two of the most common reasons food products are refused entry into the U.S. are labeling mistakes and illegal food additives? Many companies don’t discover that their products are not permitted in the U.S. market until it is too late, and they are detained at port. Any company shipping food to the

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FDEA Export Operations Webinar – Making sure your products are FDA Compliant with Registrar Corp

Organized by FDEA FDEA Export Operations Webinar with Registrar Corp Join FDEA Service Provider, Gary Baylis of Registrar Corp, as he walks you through the importance of getting your FDA registration right for exporting your products to the USA. In this webinar we will give you tips on how to ensure your products are compliant,

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MoCRA: Tips for Compliance and Preparation

The Cosmetics Direct Portal has opened and the first round of compliance deadlines for The Modernization of Cosmetics Regulation Act (MoCRA) went into effect December 2023. But many beauty brands are still in the dark about what was due, what the enforcement extension for registration and listings means, and what MoCRA deadlines are coming this year. In this webinar, MoCRA experts Don Frey and Jaclyn Bellomo, will discuss the Cosmetics Direct Portal, outline the Final Guidance for Industry and the new requirements for beauty companies—and the industry—in the months ahead.

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Calling All Beauty Brands: Have You Met MoCRA’s Compliance Deadlines?

In this webinar, global regulatory compliance leader Registrar Corp will outline what the updates and new requirements mean for beauty companies and the industry in the years ahead.

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MoCRA Requirements for Adverse Events [AM Session]

Speaker: Jaclyn Bellomo, Director, Cosmetic Services and Software

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MoCRA USA: What to Do Before the End of 2023? Organized by IFIS Cosmetiques

The Modernization of Cosmetics Regulation Act (MOCRA) was passed by the U.S. Congress and signed by President Biden at the very end of 2022.
On August 8, 2023, the FDA published a “Draft Guidance” specifying the requirements for registering establishments and reporting cosmetic products, for which, under the MOCRA law, the deadline is 12/29/2023.

In this webinar brought to you by IFIS Cosmétique and Registrar Corp Europe:
• A brief reminder of the different components of MOCRA
• Registration and listing obligations: a deadline from 2023
• Facility registration: who/what/how
• Product declarations: who/what/how
• Classic case studies
• Roadmap to prepare

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US FDA Regulations for Cosmetics and OTC drugs – Organized by COSMED

When: Tuesday, September 19 Speaker: Beatrice Muhl, Senior Regulatory Advisor Language: French Register here

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