The Parenteral Drug Association (PDA) announced it signed an agreement in February to collaborate with Deloitte Consulting, LLP and the U.S. FDA’s Compounding Quality Center of Excellence to provide training to large pharmaceutical compounders in a variety of Good Manufacturing Practices (GMP)-related functions critical to improving the overall quality of compound drugs.
PDA is offering training in areas that are core to its educational offerings, including aseptic processing of sterile drug products, environmental monitoring, and manufacturing deviation investigations and Corrective and Preventative Actions (CAPA), as well as other topics to be determined.
