Netzealous LLC DBA - Compliance4All, Online
2019-04-03
Overview: These electronic records must be maintained according to regulatory requirements contained within FDA's 21 CFR Part 11 for US jurisdictions and Eudralex Volume 4 Annex 11 for EU jurisdictions.
Why should you Attend: Attendees will learn how to review audit trails, using a risk based approach to cull through the thousands of audit trail records that can be generated on a daily basis.
Areas Covered in the Session: What is an Audit Trail 21 CFR 11 / Annex 11 requirements for Audit Trails Why Audit Trails What are Audit Trail Features What are Audit Trail Contents What records need to have an Audit Trail When does Audit Trail begin
Who Will Benefit: GxP Consultants Quality VPs IT VPs FDA Investigators Other Regulatory Agency Investigators
Event Fee: One Dial-in One Attendee Price: US $150.00
Contact Detail: Compliance4All DBA NetZealous, Phone: +1-800-447-9407 Email: compliance4all14@gmail.com
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