Webinar: Excipient GMP Differences, Risk Assessment, and Audit Findings

November 11, 2025 - 11:00am to 1:00pm EST
 
Excipients (inactive ingredients) used in drug products are required to be manufactured under an appropriate quality management system and Good Manufacturing Practices (GMP). This webinar will provide an overview of similarities and differences between published excipient GMPs as well as suggestions on risk assessment strategies to support excipient GMP implementation and documentation.  In addition, the webinar will examine and provide examples for typical audit findings for excipient products.
More information

Location

Online Instructions:
Url: https://education.ipecamericas.org/courses/107058
Login:

Contact

IPEC-Americas Staff

ipecamer@ipecamericas.org

Related Content