Valli Isabelle

Cphi North America Philadelphia 2024. Get instant access to the best in the business. This session provides an overview of the drug master file (dmf) regulatory framework and registration pathways covering active pharmaceutical ingredients (apis), excipients and packaging materials.

Purolite extends a warm invitation for you to engage with our team of experts addressing current global trends, new regulatory guidelines and our portfolio of formulation. We are creating a personalized experience for everyone at cphi north america based on their goals for attending.