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Get In Touch with a Regulatory Expert: https://www.registrarcorp.com/contact... Follow us on social media: / registrar-corp / registrarcorp X / https://x.com/registrarcorp Many LACF and acidified food manufacturers believe they are in the clear once they have registered their facility and submitted a process filing for an SID number. However, we are seeing more clients have process filings rejected by the FDA because of significant gaps in supporting documentation—gaps that often lead to returned filings, follow-up questions, or citations. Plus, the FDA has increasingly emphasized the need for a formal Process Validation Report from a Recognized Process Authority. Why this Matters For companies registering a food canning facility—or those already registered but needing a SID number—these issues can stop the process cold, delaying you from getting your product into market. In this webinar, we’ll break down the most common FDA deficiencies related to LACF and acidified food process filings and explain why many companies are surprised by FDA’s response. We’ll clarify what FDA expects to see—and where submissions most often fall short. You’ll learn: -Why a SID number does not confirm FDA acceptance -The documentation issues FDA is actively citing -What must be validated—and by whom -What FDA considers a “recognized” Process Authority -How to reduce the risk of returns, delays, and compliance setbacks If you manufacture LACF or acidified foods, this session will help you uncover potential compliance risks before they result in costly FDA action. About the Speaker: Scott Cabes is Senior Director of Low Acid & Acidified Foods at TechniCAL, a Registrar Corp company and the world’s leading independent Process Authority. With over 30 years of experience, he is a recognized expert in FDA and USDA compliance for thermally processed foods and a sought after speaker on thermal processing and regulatory compliance.