Principal Consultant, CAI
Cheryl is a professional with 42 years of experience working in FDA and ISO regulated environments. Cheryl is a certified Lead Assessor of Quality Systems and has provided training for and implemented effective compliant quality systems for oncology, cell/gene therapy, pharmaceuticals, medical devices, biologics, in-vitro diagnostics and electronics.
Cheryl is an official correspondent/U.S. Agent for foreign establishments engaged in the manufacture of pharmaceuticals imported into the US and has experience in the authoring of regulatory submissions for the US and Europe.
Cheryl can be reached at firstname.lastname@example.org