The course will assist the global bio/pharmaceutical industry providing a better understanding of compliance requirements for excipient suppliers, particularly with the USP-NF and Ph. Eur
IPEC-Americas has published the first revision of their U.S. Drug Master File Guide for Pharmaceutical Excipients
Provides best practices toward co-processed excipient development, manufacture and use, and provides support to both co-processed excipient manufacturers and users.
Overview of risk assessment tools and resources for conducting risk assessments to identify and control for potential risks to excipient quality.
Announcing the publication and availability of the revised IPEC GDP Guide
Announcing the publication and availability of the revised IPEC-PQG GMP Guide