Complying with FDA's Good Documentation Practices [It Didn't Happen]

MessageThis Webinar is over
Date Aug 13, 2019
Time 12:00 PM EDT
Cost $150.00
In a pharmaceutical or medical device environment documentation needs to 

meet certain requirements to ensure product quality and product safety.

Why should you Attend:
As the FDA and TGA say "If it isn't written down, then it didn't happen". To 

meet industry standards, it is critical that all documentation follows GDP 

when it affects:
GMP /GLP /GCP processes
Material or product identity, quality, purity, strength and safety

Areas Covered in the Session:
Document Approval
Handwritten Entries
Copies of Documents
Document Maintenance
Document Modification
Warning Letters for GDocP

Who Will Benefit:
Anyone that creates records in a regulated industry including Laboratory, 

Clinical and Manufacturing Staff, as well as IT /Software Staff

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.

Event Fee: One Dial-in One Attendee Price: US $150.00

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407


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