Thursday, 21 March 2019
5:30–8:30 pm CST
BioPharmaceutical Technology Center
5445 East Cheryl Parkway
Madison, WI 53711
+1 608 273 9737
Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) are guidelines manufacturers must follow to ensure their products meet quality standards set forth by the US Food and Drug Administration (FDA) and other regulating agencies. These guidelines are imposed for ensuring the safety and integrity of drugs and are a critical element of a good quality system. Join other regulatory professionals from your region to learn more about quality standards and how to ensure compliance.
This session is designed to provide a broad overview of the essential elements of establishing and managing quality systems. At this session, you will gain a deeper understanding of process-based quality systems, understand the similarities between GLP/GCP/GMP, identify the key hallmarks of an effective quality system and discuss examples of break downs within various quality systems.
Don’t miss this unique opportunity to learn new and innovative ways to manage risks while connecting with others from your local regulatory community. This event is hosted by the RAPS Wisconsin chapter and is intended to encourage professional development and engagement among regulatory professionals in your area. A light meal will be available for all participants and RAC holders may claim two RAC recertification credits.
Abigail Davis, MS, senior quality assurance manager, Promega
RAPS Members: $30
*Students must contact RAPS customer service (+1 301 770 2920 ext. 200), or use the student registration form to confirm status.