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Quality Management, Regulatory & Clinical Affairs –
Medical Devices & IVDs

Consulting & Documentation

Competent

Always up to date through constant qualification and extensive project experience

Pragmatic

Solution-oriented implementation of regulatory requirements without unnecessary additional expenses

Sustainable

More efficiency through transparent cooperation with my clients

With over 18 years of experience in the medical device industry, I support manufacturers and distributors of medical devices and in-vitro diagnostics in the strategic development, documentation and ongoing compliance with quality management and regulatory affairs requirements. Please feel free to contact me for a tailored and pragmatic solution.

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