Events
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The Online Seminar shows the Possibilities of the use of Desktop-Sharing Software. The Online-Seminar is free of charge an will contain the following topic. How to Setup the Software. The Webinar will held on request, the duration is approx. 30 Minutes Further Information to the Online-Seminar Autodesk is a leading manufacturer of 3D design software across a variety of different industries. This course is geared toward students who have the desire to learn the essentials of Autodesk Inventor in order to design models from sketching, solid modeling, assembly design, and drawing production. Start: 02/08/2012 8:00 am
End: 02/08/2012 11:00 am
This Process Validation training will look at the underlying statistical concepts to perform an effective process validation. The webinar examine elements of the FDA regulations for process validation (21 CFR §820.75) as well as the corresponding requirements in ISO 13485. The FDA’s Quality system regulation requires device manufacturers to validate processes when they don’t fully verify the resulting output. Based on Warning Letters, the FDA expects manufacturers to validate processes when the output check uses sampling instead of 100% inspection. The presentation looks at these aspects of process validation using the unifying approach of a statistical model. Rather than a fundamental examination of how to perform process validation, this seminar covers the tools necessary to use the statistical model. Why Should You Attend: Start: 02/08/2012 10:00 am
End: 02/08/2012 11:30 am
This 90-minute Internal Audit webinar will cover the three foundational elements that support an effective Internal Audit program - establishing Internal Audit Program objectives, developing audit plans, and writing effective non-compliances. Why Should You Attend: Internal auditing drives continual improvement and reminds everyone that Quality comes first! Auditing is an assessment tool that provides a reliable performance indicator of your organization’s system and processes. In other words, an internal audit is an audit of an entity's internal control systems and procedures and how the system and procedures are implemented. Companies that establish internal audits as part of their culture to practice discipline of process control will benefit in the long run with stable and reliable processes. In 90 minutes we will cover three foundational elements for designing an effective internal audit process. These areas include how to establish Internal Audit Program objectives, develop audit plans, and write effective non-compliances. Start: 02/08/2012 10:00 am
End: 02/08/2012 11:00 am
This Listeria Prevention training will cover HAACP requisites as well as GMP and Sanitation programs to address areas of possible listeria contamination and methods to eradicate them. Why Should You Attend: With the crisis we have seen in food safety in the last decade, deli meat, cheeses, sprouts, cantaloupe etc, QC managers are under a lot of pressure to maintain a clean sanitized facility while focusing on their HAACP plan and other crucial responsibilities. The potential for cross contamination occurs in the facility every day. Finished product is often too close to other adulterants or the adulterants can be human! This presentation will help a QC manager of a RTE processor to look through the “lens” of their HAACP and other prerequisite building blocks like strong GMP and Sanitation programs. We’ll help you see areas that the facility may be weak in and show you some tools to address, particularly sanitation, where the areas of possible listeria can be hiding, and how to clean well enough to eradicate them. Learning Objectives: Attendees will learn more about the keys to preventing listeria in the processing environment, take an in depth look at a strong sanitation program. | ||
