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Site language : English - Français
Ref : 29033
Event :Audit Trail Generation and Review 2019

Date :Wednesday April 03rd, 2019

Location :Online (Internet, Videoconferencing, ...)

Type :Education - International audience

Accreditation :--


Further information

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:
Quality VPs
FDA Investigators
Other Regulatory Agency Investigators
Speaker Profile:
Angela Bazigos is the CEO of Touchstone Technologies Inc. She has 
degrees in Microbiology and Computing and 40 years of experience 
in the Life Sciences, Healthcare & Public Health Services. 
Experience combines Quality Assurance, Regulatory Compliance, 
Business Administration, Information Technology, Project 
Management, Clinical Lab Science, Microbiology, Food Safety & 
Event Fee: One Dial-in One Attendee Price: US $150.00
Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407

Further information

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Compliance4All is a professional trainings provider for the regulated industries. It offers professional trainings for regulatory compliance professionals and offers innovative strategic consulting and advice to a broad range of organizations. These services help them to be compliant with regulatory requirements. . Compliance4All [...]

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Audit Trail Generation and Review 2019 Medicine - Bio-Technologies - Public Health - Pharmacy
education training, medical conference, technology, healthcare professionals training
Everyone, FDA Investigators Regulatory Agency Investigators
50 1 --


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