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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Compliance Secrets Top Drug Manufacturers Already Know

An insightful webinar designed for pharmaceutical manufacturers responsible for meeting FDA compliance requirements across registration, reporting, and fee-based programs. Whether you’re entering the U.S. for the first time or recalibrating your approach, this session delivers a strategic, structured overview of what’s expected—and how to get it right from the start. Topics covered: – Establishment registration

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FDA Food Inspection Preparedness: What to Expect When You’re Inspected

Watch this insightful webinar designed to help food industry professionals understand and navigate the complexities of FDA food facility inspections. This session covers: Overview of FDA Inspection Process: Learn about the different types of FDA inspections and how they decide which facilities to inspect. Preparation Strategies: Discover how to prepare your facility and staff for

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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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Réglementation canadienne sur l’étiquetage des aliments : Ce que les entreprises doivent savoir avant d’exporter

Any company that ships food in Canada must ensure that the ingredients and the labeling of its products comply with Health Canada requirements. In this webinar, Registrar Corp will outline the mandatory information that must appear on all retail food labels and describe how Health Canada regulates food products. Join us and learn how to

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Join Registrar Corp’s experts as they break down the fundamentals of medical device regulation in the United States. From device classification and 510(k) requirements to registration, labeling, and UDI compliance, this session is ideal for medical device companies looking to enter or expand in the U.S. market.

Introduction to USFDA Medical Device Regulations

Join Registrar Corp’s experts as they break down the fundamentals of medical device regulation in the United States. From device classification and 510(k) requirements to registration, labeling, and UDI compliance, this session is ideal for medical device companies looking to enter or expand in the U.S. market. #ExemptIsNotUnregulated

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Etichette e ingredienti dei prodotti alimentari per gli USA: Cosa dovete sapere per essere in regola con i requisiti della U.S. FDA

Sapevi che due dei motivi più comuni per cui i prodotti alimentari vengono rifiutati negli Stati Uniti sono errori di etichettatura e additivi alimentari illegali? Molte aziende scoprono che i loro prodotti non sono ammessi sul mercato statunitense solo quando è troppo tardi e vengono trattenuti al porto di arrivo negli USA. Le recenti normative

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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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Best Practices in Keeping Your Proprietary Information Secure When Filing with European Agencies

Discover the key requirements for Master Files (MFs) and Certificates of Suitability (CEPs) in European drug submissions—documents, fees, eCTD format, and how Registrar Corp simplifies compliance and protects your data.  

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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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Unpacking U.S. FDA Food Labeling and Ingredient Regulation: What Pacific Exporters 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. Recent FDA actions add to the

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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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Navigating the FDA Traceability Rule: Preparing for 2026 Compliance

Traceability is key to food safety, but the FDA Traceability Rule, set to take effect in January 2026, has left many in the food industry seeking answers. Navigating the FDA Traceability Rule: Preparing for 2026 Compliance will unpack the rule’s key requirements, clarify its impact on businesses—including those outside the U.S.—and address common misconceptions.  In

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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. Recent FDA actions add to the

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Are you FDA Ready? Key Requirements and Enforcement for Food Facilities

This in-depth webinar is designed to provide food manufacturers with a comprehensive overview of FDA food facility requirements and essential tips for FDA readiness. This session covers crucial topics including:   FDA Food Facility Requirements: Understand the key regulations that apply to your facility, from registration to food processing requirements and beyond.   Food Safety Plans

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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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Unpacking Canadian Food Labeling Regulations: What Companies Must Know Before Exporting

Any company shipping food to Canada should make sure their products’ ingredients and labelling are compliant with Health Canada requirements. In this webinar, Registrar Corp presents the mandatory information that must appear on all retail food labels and describes how Health Canada regulates food products. Watch now and discover how to avoid these pitfalls and

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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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FDA Food Inspection Preparedness: What to Expect When You’re Inspected

Watch an insightful webinar designed to help food industry professionals understand and navigate the complexities of FDA food facility inspections. This session covers:  Overview of FDA Inspection Process: Learn about the different types of FDA inspections and how they decide which facilities to inspect. Preparation Strategies: Discover how to prepare your facility and staff for

Read more »

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 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

Read more »

Food Safey & Labeling: Best Practices for Compliant Labels

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? 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, or they must issue a recall. Any

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Retail Therapy: Managing MoCRA compliance with Beauty Retailers

In this webinar we will take you through retailer’s expectations of MoCRA compliance and how you can continue to stay compliant not to disrupt your supply chain and distribution. What You Can Expert to Learn from This Webinar: Understanding Retailers indirect role in MoCRA Overview of Large Retailers expectations of brands compliance What documentation should be

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Practical Steps to be MoCRA Compliant Quickly

With the enforcement of MoCRA, becoming and staying compliant with new US FDA cosmetic industry regulations has never been more critical. Join us for “Practical Steps to be MoCRA Compliant Quickly” where we will empower cosmetic brands and manufacturers with knowledge and strategies to navigate the regulatory landscape in 2024 and beyond.  Our resident cosmetics

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