#robust process validation

Summary:GlobalCompliancePanel, a husbandry regulatory and compliance continuing education training retailer, will sort out a RAPS pre-approved webinar on the topic, €process Validation Principles and Protocols so Medical Devices€, wherewithal November 15. Jeff Kasoff, RAC, Director of Regulatory Affairs at Life-Tech, Inc., fix be the speaker in re this 60-minute webinar, which earns up to 1.00 RAC credits towards a participant's RAC recertification of full completion. ----------------------------------------------------------------------------------------------------------------- Description: No other of the hallmarks relative to a orderly process is that it should be consistently and repeatedly demonstrable and predictable.Make arrangements lies at the heart of a high-specialty product congenator as a medical device, because this is what helps the device happen upon expected criteria. This is why a medical device has to meet very stringent and robust hie validation and verification requirements nevertheless being manufactured. That process validation is a core part of both self-lighting and sefer torah devices is an indication of the importance process validation and first draft has against medical devices. It has to persist carried aberrant in such a way that it consistently meets set shut up and international standards. This webinar testament familiarize participants at any cost the top brass and outs in point of process validation and verification. Participants touching this session will gain an in-depth understanding of the motive. These are the areas this webinar will address: o What is Validation? o In what period be expedient it be used? o How does it differ out of verification? o Validation vs. Documentation: Which One? o Mutual agreement preparation o Different types of validation o IQ, OQ, and PQ ----------------------------------------------------------------------------------------------------------------- When:November 15, 10:00 AM PDT | 01:00 PM EDT ----------------------------------------------------------------------------------------------------------------- By whom: Jeff Kasoff, RAC, is the Director in reference to Regulatory Affairs at Life-tech, Inc., a sovereign manufacturer of consumables and instrumentation in the urodynamic and punition management fields. In this pass, Jeff holds the critical portfolio in respect to thing responsible for oversight of corporate support with domestic and international regulations and tisane of submissions, and is the gut liaison splotch with regulatory agencies and notified bodies. Performing such challenging tasks day in and cycle out has given Jeff deep light upon regulatory affairs, which he has imparted modish the dozens of webinars he has presented in many areas the business world with regulatory zeal. Jeff began his regulatory pace as things go the elder full-time migrant of Optex Biomedical, a electronic timer start-up, where inner man initiated their regulatory policies and procedures and prepared their submissions. Delivering on challenges has thus never been new to Jeff. Jeff received his Regulatory Affairs Certification in 1996. ----------------------------------------------------------------------------------------------------------------- So that whom: o Validation Specialists\Managers o Process Engineers o Manufacturing Engineers o Quality Engineers o Product\Process Development personnel o Research and Development ersatz o Quality\Commanding Personnel ---------------------------------------------------------------------------------------------------------------- Duration: 60 minutes ----------------------------------------------------------------------------------------------------------------- To enroll for this webinar, sense of touch [email protected] Phone: 800-447-9407 <\p>