A quick look at the webinar ‘Mastering the Clinical Evaluation of Medical Devices’, which took place last week!
Sandra Balseiro and Celeste Oliveira, from MDRu, provided an in-depth understanding of the regulatory requirements for clinical evaluation.
Insights from the CRO, NOVA Clinical Research Unit (NOVA CRU), helped attendees navigate the clinical evaluation process.
In addition, João Leite shared Insparya Portugal‘s first-hand experience.
This was the third in a series of webinars designed to enhance knowledge of medical device regulations: “Understanding Medical Devices Regulation”, “Software as a Medical Device and the Regulatory Implications of AI”, and “Mastering the Clinical Evaluation of Medical Devices.”