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Ali Alkhatib - Expert Regulatory Affairs & TechDoc

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Ali Alkhatib is an expert in Regulatory Affairs & Technical Documentation, with a focus on Risk Management and Usability. With a deep understanding of the digital transformation of regulatory processes, he guides medical device manufacturers from the selection and validation of suitable software solutions through to the MDR-compliant implementation of digital QM and risk management tools. His foundation is a Master's degree in Information Technology with a specialisation in Medical Engineering from Hochschule Mannheim.

Blog Post by Ali Alkhatib - Expert Regulatory Affairs & TechDoc

Dec 4, 2024 8:45:00 AM

Risk Management & Usability in Medical Devices

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May 12, 2023 8:45:00 AM

MDR Implementation: Progress, Successes and Challenges

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