The Interventional Orthobiologics Foundation is having a free webinar this coming Monday night, 6/14/21 at 6pm Pacific and 9p Eastern.
*What does the recent FDA Consumer Alert on Orthobiologics mean for Doctors, Manufacturers, and Patients?*
The panel has over 100 years combined experience in regenerative medicine AND in direct dealings with the FDA and other regulatory authorities. Sign up and listen to Andrew Ittleman Esq., Scott Bruder, MD, PhD, and Matthew Murphy, PhD as they interpret the current regulatory state of regenerative medicine in the USA.
What products are allowed? What products are not allowed?
What can I market?
Why is an IND or an IRB or Q code not enough for me to use a product?
Can I make PRP or bone marrow concentrate without a 510K device?
These and lots more will be addressed in the 1 hour seminar.
Members of the IOF Board of Directors will also be on the webinar to answer specific clinical questions.
Of all the webinars we have had since COVID, this one is a true "shouldn't miss" !