X

Stay Connected

Sign Up for Updates

 
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 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.

Recent Posts

Phased-in approach offers best hope for FDA’s proposed quality metrics program

By Camille Jackson  |    April 7, 2016
In July 2015, the U.S. Food and Drug Administration (FDA) issued draft guidance for industry requiring manufacturers to provide certain manufacturing data on an annual basis.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...   Read More

The biopharmaceutical industry’s commitment to quality

By Camille Jackson  |    February 11, 2016
America’s innovative biopharmaceutical companies are leaders in innovation and quality—not just in research and development, but also in manufacturing technology. PhRMA’s member companies implement...   Read More

Search the Catalyst

View Posts by Topic

see all

View Posts by Contributor

View Posts by Date

see all

Subscribe to Email Updates