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Getting Started: Overcoming Initial Obstacles in Medical Device Software Development
Ever wondered what it really takes for manufacturers to break into the Medical Devices market?
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What you'll learn
- Regulatory requirements for MDSW.
- Classification impact on development and documentation.
- How MDR and AI Act apply to software.
- Best practices for standards and guidance documents.
- Connections between market access, design, clinical evidence, and technical documentation.
Speakers
Join us as our expert speakers share valuable insights and practical knowledge drawn from extensive industry experience.
Don’t miss the opportunity to learn and engage with professionals in the field.
Pieter Smits
Pieter is a seasoned SaMD/MDSW expert with extensive experience in EU and US regulations and standards, especially in AI and cybersecurity regulatory requirements. His expertise covers compliance with regulations like MDR/IVDR and FDA legislation, alongside standards such as ISO 13485, IEC 62304, IEC 82304, ISO 62366, ISO 81001, and ISO 14971.
In addition to his technical expertise, Pieter brings valuable project management experience in the pharmaceutical and medical device industries, helping organizations solve complex problems and implement effective solutions to achieve their goals.
Pieter’s Mission: To prove that compliance and innovation can go hand in hand while staying at the forefront of the evolving landscape of SaMD/MDSW legislation and standards.
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