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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

Overview:
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
Email: [email protected]

Details

Date:
August 13
Time:
10:00 am - 11:30 am
Cost:
$150.00
Event Tags:
Website:
https://www.compliance4all.com/control/w_product/~product_id=502630LIVE?channel=complianceinsights_Aug_2019_SEO

Organizer

compliance4All
Phone:
18004479407
Email:
compliance4all14@gmail.com
Website:
http://www.compliance4all.com

Venue

Online Event
539 W. Commerce #1821
Dallas, TX 75208 United States
+ Google Map
Phone:
1-(214)-628-2958
Website:
https://www.trainzsmith.com/