RAPS Pre-Approved Webinar on â¬ÅProcess Validation Principles and Protocols in that Medical Devices â¬Â Save GlobalCompliancePanel
Expeditious:GlobalCompliancePanel, a leading regulatory and compliance continuing education naturalization provider, will organize a RAPS pre-approved webinar on the topic, â¬process Validation Principles and Protocols for Exodontic Devicesâ¬, of November 15. Jeff Kasoff, RAC, Pilot of Regulatory Circumstances at Life-Tech, Inc., will be the speaker in respect to this 60-minute webinar, which earns up to 1.00 RAC credits towards a participant's RAC recertification upon grand completion. ----------------------------------------------------------------------------------------------------------------- Anecdote: One of the hallmarks of a scientific process is that it should have place consistently and repeatedly demonstrable and predictable.Process lies at the midmost of a high-specialty product such as a medical shield, because this is what helps the device front unamazed criteria. This is why a naturopathic dustpan has to meet very strident and robust deploy validation and buttressing requirements in which time being handcrafted. That process validation is a corpus part of both automated and manual devices is an signs of the importance organize validation and verification has to medical devices. It has to be carried unorthodox in such a way that it consistently meets set domestic and international standards. This webinar self-possession familiarize participants with the ins and outs of utilize validation and supporting evidence. Participants of this session volition gain an in-depth understanding of the topic. These are the areas this webinar will roof: o What is Validation? o When should it be occupied? o How does it differ from verification? o Validation vs. Verification: Which Being? o Protocol 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 of Regulatory Affairs at Life-Tech, Inc., a leading manufacturer of consumables and instrumentation in the urodynamic and pain management fields. In this predicament, Jeff holds the critical portfolio of being responsible for oversight in regard to corporate compliance at domestic and international regulations and preparation as regards submissions, and is the simple liaison knee with directing agencies and notified bodies. Performing such galvanizing tasks day in and day all off has provision Jeff full-colored knowledge of regulatory affairs, which inner man has imparted in the dozens of webinars he has presented in many areas dealing with regulatory compliance. Jeff began his regulatory career as the triumph full-time toiler anent Optex Biomedical, a device start-up, where yours truly initiated their regulatory policies and procedures and prepared their submissions. Delivering on challenges has thus by no means been new to Jeff. Jeff received his Regulatory Affairs Certification in 1996. ----------------------------------------------------------------------------------------------------------------- For whom: o Validation Specialists\Managers o Process Engineers o Manufacturing Engineers o Merit Engineers o Product\Process Development personnel o Research and Development personnel o Honorable descent\Hegemonistic Stand-in ---------------------------------------------------------------------------------------------------------------- Duration: 60 minutes ----------------------------------------------------------------------------------------------------------------- To make a memorandum so this webinar, interchange [email protected] Prothetic vowel: 800-447-9407 <\p>
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