gBETA Medtech Lunch & Learn: Making Sense of the Regulatory Process for Medical Devices

Founders that enter the healthcare industry do not have an easy path ahead of them. Commercializing medical technologies can be expensive, slow and challenging due to strict regulations and compliance elements that are in place. During this FREE, Virtual talk, you will learn about FDA Product Classification, Regulatory Pathways, Quality Management, and an overview of engineering and compliance activities required for clearance.

Featured Speaker Sabrina Varanelli of Nemedio.

Register now: https://gener8tor.zoom.us/meeting/register/tJ0rfu-sqzopHdeZY4pVyW1_c_SWteOhEK2E