Corporate Regulatory Affairs, ROQUETTE AMERICAS, INC.
Priscilla has over 35 years’ experience in Regulatory Affairs and Quality for excipients, food additives and ingredients for personal care products.She is currently President of the IPEC Federation and the Vice Chair of Science and Regulatory Policy for IPEC-Americas and is also a past Chair of the organization.
This article details what co-processed excipients are and how they are made.
Viewpoint: Continued dialogue among pharma stakeholders is needed to achieve consensus regarding excipient composition.
With ingredients sold to multiple markets, excipient manufacturers must understand the different regulatory requirements for pharma vs. food.
This article seeks to encourage continued dialogue among stakeholders to achieve consensus regarding excipient additives and processing aids.
Increasingly stringent audit requirements will make third-party accredited GMP audits critical for pharmaceutical excipients and raw materials.
This article seeks to promote dialogue among stakeholders to facilitate consensus regarding requirements for excipients.
Published: April 7th 2026 | Updated: June 12th 2026
February 2nd 2021
Published: April 7th 2026 | Updated: June 12th 2026
October 2nd 2017
September 1st 2018
October 1st 2019
