MEDICAL DEVICE DEVELOPMENT MANUFACTURING. EVERYTHING IN-HOUSE.
Workshop: The Top 3 Regulatory Hurdles in Medical Device Development
Tue, Oct 29
|https://us06web.zoom.us/j/84283320479?pwd=U
Medical device inventors, join us for a one-hour live workshop and Q&A as we guide you through the Top 3 Regulatory Hurdles in Medical Device Development. Hosted by VitaTek's Senior Regulatory Specialist, Ken Meyer.
Time & Location
Oct 29, 2024, 2:00 PM – 3:00 PM CDT
https://us06web.zoom.us/j/84283320479?pwd=U
Guests
About the Event
Join us for a one-hour live workshop and Q&A as we guide you through the Top 3 Regulatory Hurdles in Medical Device Development.
VitaTek Senior Regulatory Specialist Ken Meyer will walk you through the most common hurdles when it comes to getting your medical device through the regulatory process - bring your toughest questions you didn’t want to have to pay a regulatory consultant to answer!
The workshop will consist of a short presentation on the most common hurdles and leave at least 30-min for the Q&A session.
Tuesday, October 29th
3PM EST / 2PM CST / 1PM MST / 12PM PST