Medical Devices Overview
The collection focuses on various aspects of the medical device industry, encompassing regulatory frameworks, safety protocols, clinical evaluations, and innovative technologies. It highlights the evolving landscape of medical device regulations across different countries, including the EU and India, while addressing compliance challenges and market dynamics. Additionally, there are discussions on device selection for healthcare procedures, advancements in diagnostic tools influenced by AI, and the importance of post-market surveillance to ensure ongoing safety and effectiveness in medical applications.
