BEGIN:VCALENDAR X-WR-TIMEZONE:US/Eastern DTSTART:20190806T130000 DTEND:20190806T143000 VERSION:2.0 LOCATION:OnlinePRODID:-//Training Doyens //EN METHOD:REQUEST BEGIN:VEVENT DTSTAMP:20190806T000000 DTSTART;TZID="US/Eastern":20190806T130000 DTEND;TZID="US/Eastern":20190806T143000 SUMMARY: A Systematic Approach to Human Error Reduction: Investigations, Root Cause Determination and CAPA Effectiveness DESCRIPTION: If you work in the GMP regulated industry you not only need to address human error deviations because they are an inconvenience, you must do it because the regulation requires it. The CFR - Code of Federal Regulations Title 21 Subpart B_Organization and Personnel Sec. 211.22 talks about the “Responsibilities of quality control unit” and it states that "(a) There shall be a quality control unit that shall have the responsibility and authority to approve or reject all components, drug product containers, closures, in-process materials, packaging material, labeling, and drug products, and the authority to review production records to assure that no errors have occurred or, if errors have occurred, that they have been fully investigated…” That being said Human Error is NOT a root cause. Human errors start at the design stage. From procedures, training, and workplace environment many variables that affect human behavior CAN be controlled for human error reduction. To work with these challenges, it is essential to understand human behavior, the psychology of error and root causes for human error deviations as well as implementing a process exclusively dedicated to investigating and “fixing” these problems. This human error prevention training offers practical approaches and models for addressing and controlling human error in GMP related environments by using a particular methodology to correct, prevent and avoid reoccurrence of these matters. PRIORITY:3END:VEVENT END:VCALENDAR