Medical Devices Regulation

Related lectures (31)

Page 3 of 4

Explores the principles and examples of the design review process, emphasizing documentation, risk analysis, and verification.

Explores the regulation of therapeutic products, covering legal requirements, product classification, market access, and advertising rules.

Covers the importance of user input in defining requirements and developing user stories.

Covers practical image processing using Fiji software, emphasizing data quality importance.

Discusses the circuit block diagram and design requirements for neural amplifiers.

Explores the shift from software testing to formal specifications, highlighting the significance of clear requirements in software engineering.

Introduces image processing with ImageJ and Fiji, covering installation, plugins, and tools for analyzing and measuring images.

Explains design scenarios, requirements, and a wine recommendation case study.

Covers software engineering essentials, emphasizing requirements, modularity, and abstraction, with practical insights and examples.

Covers the development of soft grips for delicate sample testing in tension, including design, analysis, and commercial strategy.