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Alternative Food Preservation: Pasteurization
Dr. Tatiana Koutchma
60 Min
Product Id: 701886
In this Food safety training learn about Food preservation, traditional heat treatment, emerging food processing technologies, pasteurization, shelf life extension, acid and low acid foods, US FDA and USDA regulations, Health Canada, new regulatory terms and definitions, novel foods, high hydrostatic pressure, ultraviolet light, microwave heating, pulsed electric fields.
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Record Keeping for a food Recall: Keeping Records to Minimize the Affect of a Recall
Craig Nelson
60 Min
Product Id: 701119
This Food safety training will provide valuable guidance to management, supervision, and quality staff that are involved with record keeping for product and ingredient traceability and recall.
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Record Keeping for the Bioterrorism Act: Meeting and Exceeding the Requirements in a Simple Manner
Craig Nelson
60 Min
Product Id: 701318
This Bioterrorism act training will provide the attendee a clear understanding of what is expected, how an investigation will proceed, and how to keep records that will minimize the impact of an incident.
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HACCP in a Real World Environment
John Miller
60 Min
Product Id: 701173
This HACCP training will explain the FSIS regulations and policies program requirements.
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Rules of Practice (FSIS) 9CFR part 500
John Miller
Product Id: 701172
This Food Safety and Inspection Service (FSIS) training will guide you through the different levels of enforcement that FSIS utilizes.
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Critical Control Points (CCP’s). Where are they? Why? When?
Irwin Pronk
60 Min
Product Id: 701180
This Food safety compliance training will explain the CCP Decision Tree and help you understand the principles behind each question. We will review various food processing steps in a variety of situations to determine whether they are CCP’s. What is the thought process in determining a CCP? Can it be done consistently? What criteria are used? Are some processing steps always CCP's e.g. heating? If not, why? One thing to remember is the importance of analyzing the hazards at each step very carefully. The more clearly the hazards are described (including equipment failures, personnel errors etc) the easier it will be to find the CCP.
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Validation & Verification: Differences between USDA and Codex
Irwin Pronk
90 Min
Product Id: 701179
This Food safety compliance training will help you understand the significant differences between the two words and even multiple meanings of the term ’Verification’. Between USDA and Codex there are slight differences and on top of that the definitions have changed over the years. It is very easy to get confused. By going back to principles, referring to other standards (e.g. ISO9000) and simpler terminology students will clearly understand the intent of both Validation and Verification. Having clarified the intent and principles we will review examples of Verification in both Prerequisite Programs and CCP's.
Validation will be explained, especially as it relates to validation of CCP's though the concept pervades the entire HACCP process. Examples will include Cooking, Cooling, and Allergen Cleaning. We will also discuss the two aspects of Validation; the product risk (microbiological, chemical or physical) as well as the Capability of the process. Both must be understood to ensure the control of CCP's is robust. Methods to verify the entire HACCP System will be covered and how this is different from verifying Prerequisite Programs and CCP's.
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The CAPA Trap or Common Problems and Pitfalls
Jeff Phillips
60 Min
Product Id: 700914
The following webinar will cover common CAPA problems across industries and how to avoid them. This webinar will provide valuable assistance to all regulated companies that need to have CAPA systems as mandated by the FDA.
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Applying HACCP to insure compliance
Joyce Wilkins
60 Min
Product Id: 700466
This HACCP training will equip the student to apply the concepts of HACCP in their food operation in a manner that is useful and effective without being unduly burdensome. Although HACCP has been around for over 40 years, it still remains the standard in designing a food safety program.
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Getting to Know FDA Audit Practices and the 10 Most Common Cited GMP Deficiencies
Kenneth Christie
Product Id: 703635
This training program will provide attendees with a better understanding of how the FDA conducts their audits and the areas of most focus. In addition, it provides a summary of common GMP deficiencies given to drug manufacturers, to use to evaluate one’s own practices. Finally, when given a regulatory audit finding, this webinar will review the top five items to remember when submitting your responses to them to avoid further questions.
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Key Factors to Develop an Effective CAPA System
Kim Huynh-Ba
Product Id: 703320
This training will focus on the regulatory requirements for a Corrective and Preventive Actions (CAPA) system. Attendees will learn how to develop an effective CAPA system.