FDA`s 21 CFR 11 Add-On Inspections - Recent Updates 2013

FDA`s 21 CFR 11 Add-On Inspections - Recent Updates 2013 is a webinar that covers topics such as:

• What are the inspection trends?
• What is FDA`s most current thinking related to computers and electronic records?
• What are the most frequent deviations for computer system validation?
• What are most frequent recent citations for Part11?
• How important is risk based Part11 compliance?
• Under which circumstances can inspectors exercise enforcement discretion?

FDA`s 21 CFR 11 Add-On Inspections - Recent Updates 2013 brings together attendees from FDA Regulated Environments, including IT Manager and Staff, FDA Regulated Environments, Regulatory Affairs, QA Managers and Personnel, Consultants, Training Departments and Validation Specialists.