Best Practices in 21 CFR Part 11-Advanced Level

Venue: San Francisco

Location: San Francisco, California, United States

Event Date/Time: Feb 03, 2003 End Date/Time: Feb 04, 2003
Early Registration Date: Jan 03, 2003
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Providing advanced level training for complying with electronic regulatory submissions and 21 CFR Part 11, this training course encompasses many hands-on interactive exercises and discussions, as well as innovative case studies. Determine which hardware and software systems are subject to regulatory inspections and examine FDA inspection trends related to computerized operations. Ensure compliance-related corrective action responsibilities are put in practice to prevent any warning letters from the FDA. Overcome common validation obstacles for computerized laboratory and manufacturing operations. This comprehensive advanced level training course critiques Part 11 and trains the advanced professional to improve foundation practices that support regulatory compliance. Attending this two day training course will help save manpower, time, and cost for your company.