Dr. Claudia Rampp, Senior QA and RA Manager

Dr. Claudia Rampp has supported clients since 2017 with regulatory questions and quality management in the development and approval of medical devices and in vitro diagnostics. Previously, she spent 16 years at a global biotechnology company developing automated systems for life sciences and molecular diagnostics.

As a trainer at the qtec Academy, Claudia Rampp focuses primarily on development-related topics such as design control, risk management, and usability.

What matters most to her as a speaker:
"Development requires out-of-the-box thinking. Regulatory requirements and quality management are often seen as limiting. I want seminar participants to gain practical benefits from my training and to look forward to implementing what they've learned in their companies."