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Connie Landaverde, Ph.D.

Connie Landaverde, Ph.D.

Regulatory Affairs Professional

Pharmaceutical / Bio-tech

Los Angeles, Los Angeles

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About Connie Landaverde, Ph.D.:

I have worked in the biotech industry for over 15 years in diagnostics and pharmaceuticals. I have over three years of experience in regulatory affairs and have been highly involved with chemistry, manufacturing, and controls documentation and submissions to the FDA. I have authored and compiled Module 3 sections of regulatory submissions.

Experience

-Biotech industry for 15 years

-12 years was assay development scientist and 3 years regulatory affairs

Education

I have a Ph.D. from University of Southern California in Biochemistry and Molecular Biology

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