Webinar NeuroTech Devices: Regulatory, Preclinical, and Clinical Insights

Are you navigating the right evidence and strategy to advance your neurology medical device? 

Developing neurological medical devices requires early alignment across regulatory strategy, preclinical and clinical evidence to avoid costly delays and rework. In this webinar, NAMSA regulatory, preclinical, and clinical experts specializing in neurology will share practical considerations and real‑world insights to help device companies anticipate challenges and make informed decisions throughout the development process. Attendees will gain a clearer understanding of how to align requirements and expectations across the product lifecycle.

Key Learning Objectives:

• Regulatory considerations for neurological devices, including strategy and FDA expectations
• Preclinical considerations for neurological devices, including study design and model selection.
• Clinical considerations for neurological devices, including site logistics and recruitment strategies