Category: On-Demand Webinar

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

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

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

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

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

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.

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

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

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

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

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

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

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

Join this webinar to meet Foodsteps, the latest company to join the Registrar Corp portfolio. Foodsteps helps food services companies and food manufacturers accurately measure, reduce and report their environmental impact.    In this webinar you’ll learn about:  Mandatory and voluntary sustainability requirements that may apply to your business (like SBTi, FLAG, and CSRD)  Essential strategies

Join us for an in-depth webinar series designed to provide food manufacturers with a comprehensive overview of FDA food facility requirements and essential tips for FDA readiness. This session focuses on the various Food Safety Plans and Programs to help safeguard your food operations, including: Food Safety Plans Supply Chain Program Recall Plans HACCP Plans

Expert Jaclyn Bellomo will take you through an introduction to the FDA’s expanded authority and regulatory power concerning Adverse Events in cosmetics. This new requirement will significantly impact how companies handle health-related consumer reports, as the FDA can request records if there is a reasonable probability of causing a serious adverse health consequence or public

With sustainability and innovation on one side and rapidly shifting consumer behavior on the other, the Beauty and Cosmetics industry is experiencing a profound transformation. Companies are working to meet these demands while also navigating evolving regulatory requirements.   This webinar will delve into the critical trends shaping the future of Beauty and Cosmetics packaging and

Join us for an in-depth webinar series designed to provide food manufacturers with a comprehensive overview of FDA food facility requirements and essential tips for FDA readiness. This session will cover crucial topics including:   -FDA Food Facility Requirements: Understand the key regulations that apply to your facility, from registration to food processing requirements and

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

FDA has expanded authority and regulatory power specifically for Adverse Events. FDA can now issue a Mandatory Recall if they determine that a cosmetic product is adulterated or that the exposure will cause serious adverse health consequences. They can also suspend a facility if there is reasonable probability of causing a serious adverse health consequence

Last year 51% of U.S. food importers audited by the FDA failed – mainly due to an inadequate Foreign Supplier Verification Program (FSVP). Businesses that don’t comply with complicated FSVP regulations are putting themselves at risk of costly penalties and supply chain disruptions.   In this webinar, FSVP compliance experts Coley Anderson and John Kelly will

This webinar will take you through an introduction of the requirements of 21 CFR 58, Good Laboratory Practices for Nonclinical Studies and give you valuable examples of why GLP is important in a lab setting while identifying if the regulation applies to you and your company. We will also give you key strategies for implementation

Discover the essentials of Master Files (MFs) in the drug industry with our experts, Melissa Sayers and Megan Moore. Learn about which agencies utilize MF submissions, what are the common required documents, when fees apply, and the submission processes. We’ll also cover electronic Common Technical Document (eCTD) submission, a common format for MFs, and how

Você sabia que dois dos motivos mais comuns pelos quais os produtos alimentícios são proibidos de entrar nos EUA, são erros de rotulagem e aditivos alimentares ilegais? Muitas empresas não descobrem que seus produtos não são permitidos no mercado dos EUA até que seja tarde demais, e eles são detidos no porto. Qualquer empresa que