Food and Dietary Supplements Regulatory Compliance Training - Live Webinars, Recordings & CDs

This webinar on the regulation of common materials used in food packaging will feature relevant elements of 21 CFR as well as USFDA guidance documents pertaining to the subject matter. It will help attendees understand the process and plan for packaging regulation as an integral part of product development efforts.

This webinar will provide an overview of the relevant statutes, including the Food and Drugs Act and its regulations and the Consumer Packaging and Labeling Act and its regulations. Core labeling requirements will be outlined and discussed, as will the rules around making voluntary label claims. Finally, an overview of Health Canada’s modernization makeover as it relates to labeling will provide insight into possible future reform, including proposals relating to the nutrition facts table and ingredient list.

In this Food Safety training learn how to create and implement a sanitation SOP to avoid failure of the HACCP system.

This training program will discuss why it is important for you to be better aware of and to become better acquainted with FDA inspection best practices. In particular, the webinar will detail a list of Dos and Don’ts before, during and after the inspection.

This webinar will teach attendees how to prepare for, manage, and follow up on FDA inspections. It will discuss common pitfalls to avoid during an inspection.

This dietary supplements quality compliance training will review the FDA regulatory requirements for manufacturing and commercialization of dietary supplements. You will gain a complete understanding of FDA requirements for manufacturing of nutraceuticals, food drugs, and dietary supplements.

Health Canada takes an active role in ensuring compliance with the regulatory requirements for advertising, marketing and selling food in Canada. In addition to rules to ensure the safety of food for Canadians, there are strict rules to ensure that manufacturers do not make false or misleading representations about food to Canadian consumers. This training program will introduce participants to various key legislations and its regulators, and discuss regulatory measures to ensure compliance.

The global regulatory environment for tobacco, e-cigarette and e-liquid products is rapidly evolving as legislators and regulators in the United States, European Union and Asia attempt to understand the health and safety concerns presented by these novel products, and develop appropriately tailored laws and regulations. This training course will present an overview of e-cigarette regulations in Asia, the European Union and around the world. It will also detail the key provisions of FDA’s deeming regulations.

This webinar will provide guidance on how to develop and implement an effective cleaning validation plan, customized for specific scenarios, to ensure that the allergen is removed from the food processing line or equipment.

This trade webinar will explain the complex US entry process so companies that import FDA regulated products will benefit from a better understanding of how the process works. It will discuss factors and actions that can lead to an import shipment being delayed or not allowed entry into the USA.

This food safety webinar will provide an overview of the Safe Food for Canadians Act, and will highlight some of the key elements we are likely to see in the regulations and expected to impact imports and exports. These regulations are scheduled to be introduced in draft in the Fall, with implementation targeted for mid-2015.

This webinar will offer participants an understanding of the Tobacco Control Act, modified risk tobacco products and how FDA’s Deeming Regulation for currently unregulated products should be tailored for tobacco products depending on where they fall under the continuum of risk.

This webinar will provide valuable education and assistance to all regulated companies that need to develop or improve their product recall and crisis management systems, including companies in the produce, meat and processed food fields.

This webinar will summarize the regulatory requirements for FDA’s proposed new regulation – “Current Good Manufacturing Practice and Hazard Analysis and Risk Based Preventative Controls for Human Food” - 21CFR Part 117. The GMP component of this regulation (Subpart B) is intended to replace the current outdated GMP regulation (21CFR Part 110) when it becomes effective, as expected, in 2015.

Although FDA's Dietary Supplement Current Good Manufacturing Practice (CGMP) Final Rule 21 CFR Part 111 has been enforced since 2010, manufacturers, distributors and importers are still not completely aware of its impact. This webinar will highlight best practices for implementing 21 CFR 111 for dietary supplements.

This webinar on good warehousing practices for human food will provide an introduction to FDA regulation requirements and proper procedures for food storage. It will emphasize the importance of proper storage procedures to avoid contamination of food that can cause illness or death. It will explain how FDA acts during and after inspections of food warehouses storing adulterated foods to ensure compliance with the FD&C Act and how warehouse facilities can ensure regulatory compliance.

This webinar will cover in detail the current Good Manufacturing Practices (cGMPs) regulations for pharmaceutical products. Attendees will learn how to comply with these FDA regulations and avoid pitfalls.

This food safety webinar will explain how to thoroughly review a food contact substance, determine its regulatory status and obtain a new regulation from FDA via the FCN process for a substance that does not meet suitable regulatory status.

This webinar will explain cGMP regulations for dietary supplements. It will provide an overview of key requirements for dietary supplements including written procedures and records required by cGMP. Attendees will learn best practices to comply with these regulations.

This webinar will focus on ISO 22000 Food Safety Management System and its comparison to the Global Food Safety Initiative (GFSI) Standard. It will provide an overview of key requirements and will discuss differences and similarities between both the approaches. It will also address key strategic business factors to consider when selecting a particular approach.