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Tuesday, August 26, 2014
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Webinar on Quality System Regulations (QSRs) for Medical Devices and IVDs
August 26, 2014 from 1pm to 2pm – Online FDA states in warning letters “This inspection revealed that these devices are adulterated within the meaning of section 510(h) of the FD&C Act, in that the methods used in, or the facilities or… Organized by compliancetrainings | Type: webinar
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Live webinar on FDA’s 21 CFR Part 11 Add-on Inspections
August 26, 2014 from 1pm to 2pm – Online In December 2010 the FDA began a project to better understand the industry’s adherence (or lack thereof) to 21 CFR Part 11. This involves the add on’ surveillance inspections of the sponsors’ compute… Organized by compliancetrainings | Type: webinar
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