Why Should You Attend:
Federal regulation of food contact materials has evolved extensively over the past 20 years. Founded on the Federal Food Drug and Cosmetic Act, Food and Drug Administration Modernization Act, and enumerated in 21 CFR 170-186 and numerous guidance documents, the regulations are complex. Ultimately, avoidance of the need for filing a Food Contact Notification (FCN) is the goal; however product stewardship and marketing concerns may preclude this outcome.
Determining the regulatory status of polymers and paper used in food contact is a stepwise process taking advantage of principles of chemistry, toxicology, engineering and risk assessment. Obtaining a new regulation from FDA via the FCN is not always necessary. This webinar will highlight the stepwise process. It will explain the complexities of various regulations of food contact materials with specific examples and case studies.
Areas Covered in the Webinar:
Who Will Benefit:
Packaging manufacturers as well as food manufacturers and facilities responsible for packaging/labeling food products will benefit from this training. Specifically, those who will benefit include individuals with R&D, Marketing and Regulatory responsibility at:
Dr. Jeffrey Scott Eberhard’s 19 year career has been spent supporting clients in their efforts to bring heavily regulated products to market. At Morton International (now part of Rohm & Haas) and Covance, he was responsible for directing and performing studies designed to generate data in support of Food Contact Notifications (FCN), Threshold of Regulation opinions (TOR), Food Additive Petitions (FAP) and Color Additive Petitions. With many of these products, he worked closely with client Regulatory and Marketing personnel, as well as client customers, to make sure that marketing’s proposed product claims were supportable and client requirements were met.
In Washington, DC working as a Staff Scientist for Keller and Heckman, Dr. Eberhard developed a high level of expertise in the regulation of Direct, Secondary Direct and Indirect Food Additives by FDA and many of their international counterparts (EU, Canada, MERCOSUR, Japan, China, and South Korea). Later, at Exponent, Nerac and ERM, he brought experience gained at Keller and Heckman and developed new competencies. In addition to the food additive, food contact, pesticide and chemical work, Dr. Eberhard prepared Generally Recognized as Safe petitions for self-certification and submission to FDA.
Our refund policy is governed by individual products and services refund policy mentioned against each of offerings. However in absence of specific refund policy of an offering below refund policy will be effective.
Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange. Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time. On-Demand Recording purchases will not be refunded as it is available for immediate streaming. However if you are not able to view the webinar or you have any concern about the content of the webinar please contact us at below email or by call mentioning your feedback for resolution of the matter. We respect feedback/opinions of our customers which enables us to improve our products and services. To contact us please email [email protected] call +1-888-717-2436 (Toll Free).
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