08/12/2021
By Grace Callen
Demystifying Medical Device Classification & Approval with MITRE
by FORGE - From Prototype to IMPACT
Join via Zoom. Note: This event WILL be recorded.
Date: Aug. 19, 2021
Time: 10 a.m.
Medical device startups, are you struggling to understand FDA regulations? Join our webinar with not-for-profit organization MITRE for help.
Medical device startups, are you struggling to understand the Food and Drug Administration’s (FDA) regulatory rules? Are you unsure of your product’s proper class and approval process? How to make sure you’re obtaining proper clearance? Join our open webinar with not-for-profit organization MITRE on August 19th 10-11 AM for guidance.
Although establishing your product’s class and moving through the regulatory pathway is a required for FDA clearance, the process is not always straight forward. Operating multiple federally funded R&D centers, MITRE’s is on a mission to “work in the public interest to discover new possibilities.” FORGE is partnering with MITRE to host this free educational webinar so that more life-saving devices can get to market faster.
All startups will have the opportunity to ask MITRE experts specific classification questions about their devices during this one-hour session. We welcome any and all startups with physical products or components to join this event. The Program Manager at FORGE, Anya Losik, will be moderating the event to ensure the best experience possible. Please register and get answers about your medical device classification and regulatory pathways concerns.