We are creating a place where we can share ideas, provide the perspective of America's biopharmaceutical companies and, most importantly, listen to you.
Camille Jackson Camille is a Senior Director of Science and Regulatory Advocacy at PhRMA. An experienced scientific program administrator, Camille has worked with academia, government, non-profit organizations, and the pharmaceutical industry. She currently serves as the PhRMA coordinator for regulatory harmonization efforts within the International Conference on Harmonization (ICH) and the program manager for global quality and manufacturing initiatives.
In July 2015, the U.S. Food and Drug Administration (FDA) issued draft guidance for industry requiring manufacturers to provide certain manufacturing data on an annual basis. The FDA’s Center for...