Medical Device
Unlock the potential of medical device innovation with Amorit Education's webinars. Our focused sessions provide insights into the latest regulatory standards, technological advancements, and market trends, guiding professionals through the complexities of the medical device industry for enhanced patient care and product development.
Preparing a FDA 510(k) submission - What to Know in 2024
Overview: The FDA 510(k) submission process remains one of the most crucial regulatory pathwa..
Date : 29th October 2024
Time : 1:00 PM Eastern Time / 10:00 AM Pacific Time
Duration : 75 Mins
Business Process Mapping – How to Prepare a Detailed System & Data Roadmap for a Clinical Trial Regulated by FDA
Overview: Conducting human clinical trials requires strict adherence to government regulatory ..
Date : 30th October, 2024
Time : 1:00 PM Eastern Time / 10:00 AM Pacific Time
Duration : 90 Mins
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