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Posted: Thu 5:07, 24 Oct 2013 Post subject: jordan pas cher Raps Pre-approved Webinar On curre |
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Description:
This webinar talks about the current Good Manufacturing Practice (cGMP) for medical devices, including in vitro diagnostic medical devices.
All medical devices are subject to Good Manufacturing Practice (GMP). This session will familiarize participants with the Current Good Manufacturing Practice (cGMP) present in the medical devices industry. This includes in-vitro medical devices. This session will also proffer guidance on the cGMP requirements as stated in the Quality System Regulations (QSRs), which ensure that medical devices are safe and effective for their intended use.
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By whom:Dr. David Lim is a certified professional for regulatory affairs (RAC) and also is a certified quality auditor (CQA) by the American Society for Quality (ASQ). Dr. Lim obtained his Ph.D. in biological sciences at the University of Missouri-Columbia and published his thesis research in the prestigious journal, Science.
Dr. Lim is an auditor, regulatory coach, consultant and instructor for global matters pertaining to regulatory affairs and compliance, quality and clinical affairs. He is familiar with more than 200 medical products (medical devices including IVD products, biologics, drugs and combination products).
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Duration: 60 minutes
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To enroll for this webinar, contact
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