eSTAR 5.0 - Are You Ready?

I know there's been a LOT of information coming out about eSTAR 5.0 lately, but that's because it's confusing. And frustrating. And imperfect.

Much like the FDA itself. 😁

But if you missed my eSTAR 5.0 webinar earlier this month, here's your chance to catch it - in all its regulatory glory.

And check out the podcast Q+A session with Patrick Axtell from the FDA:   / rqdts  




Keywords: medical devices, medical device regulatory affairs, medical device regulation, regulatory affairs, regulatory affairs medical devices, regulatory compliance, FDA, medtech, biotech, regulatory consultant, FDA submissions, 510k submissions, 510k