["Director QA/QC GLP In Vivo Operations", "RPM ReSearch"]

Can you provide an overview of your experience with Good Laboratory Practice (GLP) compliance and how it applies to in vivo research?

Describe your familiarity with FDA regulations, specifically 21CFR Part 11. How have you ensured compliance with these regulations in previous roles?

Have you conducted audits and inspections to assess compliance with GLP standards and regulations?

Do you have experience training and educating research staff about GLP principles, FDA regulations, and 21CFR Part 11 compliance?

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