BEGIN:VCALENDAR X-WR-TIMEZONE:US/Eastern DTSTART:20200421T130000 DTEND:20200421T140000 VERSION:2.0 LOCATION:OnlinePRODID:-//Training Doyens //EN METHOD:REQUEST BEGIN:VEVENT DTSTAMP:20200421T000000 DTSTART;TZID="US/Eastern":20200421T130000 DTEND;TZID="US/Eastern":20200421T140000 SUMMARY: Data Integrity for the Laboratory and Beyond - Careful Considerations for Your Next Audit DESCRIPTION: Data integrity is the assurance that data records are accurate, complete, intact and maintained within their original context, including their relationship to other data records. This definition applies to data recorded in electronic and paper formats or a hybrid of both. To assure the quality of raw materials, in process materials and finished goods, laboratory data integrity is assuming greater importance in current Good Manufacturing Practices (CGMP) for US Food and Drug Administration (FDA)-regulated industry. Data integrity and security infractions are not only 21 Code of Federal Regulations (CFR) Part 11 issues but also severe CGMP violations. The reasoning behind this complex issue is quite simple: if the integrity of laboratory data is compromised, batches of finished goods may not comply with regulatory authorization terms and, consequently, will not be released for sale. PRIORITY:3END:VEVENT END:VCALENDAR