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Explores the regulation of medical devices in Europe, covering market authorization, risk classification, conformity assessment, and post-market surveillance.
Explores European regulations for medical devices, covering classification, manufacturer's role, post-market follow-up, and essential requirements compliance.
Explores the fundamentals of requirements definition in systems engineering, emphasizing the importance of clear and concise requirements for successful system design.
Explores the history, definitions, and challenges of Systems Engineering, emphasizing the importance of requirements in system design and architecture.
