Why Should You Attend:
Historically, FDA has not had authority to collect fees from the food industry for any reason (except in the case of a court-ordered seizure of product which violates the Federal Food, Drug, and Cosmetic Act. FSMA does not authorize fees for food additive petitions or other applications for FDA approval for food additives.
The authorization is to offset FDA costs of facility re-inspections after violations; costs to FDA of a recall if the responsible company refuses an FDA recall order; and the costs of re-inspection of food offered for import which appears to violate the Act.
Areas Covered in the Webinar:
Who Will Benefit:
Ralph A. Simmons has over 35 years of experience in FDA regulation of food, and related products such as direct food additives, and food-contact substances. This experience has included the representation of companies with FDA-regulated products and experience as a senior policy advisor within FDA. The experience in FDA included work on regulations to implement FSMA.
Mr. Simmons has extensive experience in working with FDA on FSMA regulations and regulations in related areas, such as direct food additives and food-contact substances. This experience has included representing industry in negotiations with FDA, which avoided having food-contact material suppliers being registered under FDA’s program of registration of food facilities, located domestically and internationally.
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