Course Dates Upcoming Dates and Locations Virtual seminars run as 1/2-day sessions. In-person classes run as full-day sessions. See the virtual session daily class times. There are no public training classes scheduled right now but this class can be delivered privately to 6 or more people at any time. Ask us for details!
Course Details What Will You Learn At the end of this workshop, you will be able to: Describe 21 CFR Part 11 requirements for electronic records and signatures Describe US regulatory expectations and guidance for data integrity ALCOA+ Examine how to implement risk-based and critical thinking to apply the best approach to a specific system Who Should Attend Anyone in a pharma organization responsible for managing procedures, approvals, and data in electronic form. All RA/QA professionals and other cross-functional team members. Virtual Half-Days In-Person Full-Days CEUs 0.8
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