FDC Members include quality control and assurance, regulatory and compliance, scientific, engineering, manufacturing, marketing and sales professionals from companies, industry consultants and service organizations concerned with food, pharmaceuticals, cosmetics and related products.
Event name: ASQ FDC Workshop ~ FSMA Series
Date: May 15, 2019
10 am - 2 pm
Location: Glendale Learns
1255 South Central Avenue
Glendale, CA 91204
Description: The Intentional Adulteration regulation requires that individuals identifying and explaining mitigation strategies “have successfully completed training for the specific function.” This training, developed by the FSPCA, is the “standardized curriculum” recognized by FDA that will prepare you to complete the test and get a certificate. You need to score 80% or higher to get a certificate.
Midwest FDC presents: "Understanding the FDA's Expectation for Documentation"
The FDA didn't think industry had a firm grasp of their expectations, so they created a Guidance for Industry entitled Data Integrity and Compliance with Drug CGMP. Our speakers will address the Data Integrity Guidance for FDA-Regulated I industry followed by discussion delving a little deeper into expectations for SOP content, Investigations, and Change Records.
Join us for this discussion on Wednesday, June 19, 2019, 8 am - 11 am at Harper College in Palatine, Illinois.
Register at https://fda_documents.eventbrite.com
Come visit the ASQ FDC booth at the 123rd AFDO Annual Educational Conference,
Atlanta, GA | June 22-26,2019.
For more information and registration, click here: https://afdoconference.org/
Mark Your Calendar!
Midwest FDC "Data Integrity Conference"
Harper College, Palatine, Illinois
Wednesday, September 18, 2019
Midwest FDC - "Networking with the FDA"
Stonegate Conference Center, Hoffman Estates, Illinois
Tuesday, November 12, 2019
5 Things Pharma Managers Need to Know about ISO 9001:2015
by Elena Mack
Certified HACCP Auditor (CHA) Video Preparation Course
Basic Quality Tools applied to the Food Industry
by Aura Stewart
Free Webinar for FD&C Members
ISO 9001 Recorded Webinar
The Certified Pharmaceutical GMP Professional Handbook
The Reproducibility Crises in Biomedical Research and its Impact on Pharmaceutical R&D Productivity
by Ulo Palm, MD, PhD.
Medical Device Human Factors-Catching up to the FDA (Youtube)
by Korey Johnson, Associate Director of User Centric
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