Auditing Systems for 21 CFR Part 11 Compliance – Webinar By ComplianceOnline
| June 14, 2012 |
Online Event
This webinar will present a methodology for system assessment, risk-analysis, 21CFR Part 11 compliance, remediation and inventory, along with templates and forms that attendees can modify for their own business. Read more »
Overview: This course will present the latest on FDA thinking (with slides directly from the FDA’s Office of Compliance), discuss how these inspections will impact both your company and the industry, and provide guidance on how your company can ensure that they have a successful inspection.
This webinar will give a good understanding of FDA and international expectations for auditing computer systems and provide steps for cost-effective implementation.