Category: On-Demand Webinar

Drug registration and listing renewals are non-negotiable for maintaining FDA compliance—and missing even one step can result in product inactivation or regulatory action. This webinar is designed for manufacturers, private labelers, and compliance professionals who need clear, actionable guidance on staying ahead of FDA requirements. Our experts will break down what’s required, what’s commonly missed,

Registrar Corp and the U.S. Commercial Service of the U.S. Embassy in Australia hosted an exclusive webinar tailored for food and beverage exporters across Oceania looking to enter and succeed in the U.S. market. This session will feature opening remarks from senior representatives of the U.S. Commercial Service and Austrade, followed by expert insights from

Overview of two of FDA’s most effective enforcement tools: detention in port and import alerts. We will discuss how and why products are detained and circumstances under which the detention can be resolved and the products released. We will also discuss FDA’s system of import alerts, why companies are placed on import alerts, and how

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

Avoid Costly Delays and Master the FDA Import Process for Drugs and Devices. Drug and device shipments are often delayed or denied entry into the U.S. due to issues like incomplete documentation, labeling mistakes, or active Import Alerts. For companies importing FDA-regulated products, a solid understanding of the import process—and how to effectively respond to

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.

Join us for an in-depth webinar designed for medical device manufacturers navigating FDA requirements related to product labeling, traceability, and Unique Device Identification (UDI). Whether you’re preparing your first UDI submission or reassessing your compliance program, this session offers a structured, strategic overview of what the FDA expects—and how to implement it correctly across your

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

Join us for an in-depth webinar examining the future of food ingredient regulation in the United States in light of recent public statements by HHS Secretary Robert F. Kennedy Jr. directing FDA to explore rulemaking that could eliminate the current system allowing food companies to self-affirm substances as “Generally Recognized as Safe” (GRAS) without FDA

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

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

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

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

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

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

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

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

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.  

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,

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

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