SciLucent’s staff includes scientific, medical, and regulatory professionals with expertise and experience in all aspects of healthcare product development and marketed product support.
Kelley C. Boyer, M.S.
Preclinical Program Development and Implementation; Regulatory Strategy, Documentation, and Implementation
Kelley Boyer specializes in providing nonclinical product development support. She prepares regulatory submissions and GLP-compliant study reports for the development of pharmaceuticals and biologics. Kelley monitors nonclinical studies to ensure that they are conducted using current technologies and are in compliance with Good Laboratory Practices. Kelley is a trained technical writer with significant expertise in genetic and molecular toxicology.
