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Complying with FDA’s Good Documentation Practices [It Didn’t Happen]
August 13 @ 10:00 am - 11:30 am CDT$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:
Copies of Documents
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
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
Compliance4All DBA NetZealous,
Email: [email protected]