EU MDR And Medical Device Regulatory Affairs Specialist
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Englisch, Deutsch, Französisch, Italienisch
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Über mich
I help medical device manufacturers, startups, and healthcare businesses achieve regulatory compliance with confidence. I specialize in EU MDR documentation, EUDAMED, MHRA registration support, Technical File preparation, ISO 13485 documentation, device classification, risk assessment, and regulatory compliance. My focus is delivering accurate, confidential, and high-quality work with clear communication and on-time delivery.... Mehr lesen