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.




Best Practices in Preparation for an FDA Computer System Audit in 2024

Best Practices in Preparation for an FDA Computer System Audit in 2024

Overview: The FDA mandates that all computer systems used to produce, manage, and report on “..

Date : 22nd July 2024

Time : 1:00 PM Eastern Time / 10:00 AM Pacific Time

Duration : 90 Mins

21 CFR Part 820 - Quality System Regulation - Applying Principles of Lean Documents and Lean Configuration

21 CFR Part 820 - Quality System Regulation - Applying Principles of Lean Documents and Lean Configuration

Overview: 21 CFR Part 820 delineates the Quality System Regulation (QSR) that governs all ent..

Date : 23rd July 2024

Time : 1:00 PM Eastern Time / 10:00 AM Pacific Time

Duration : 75 Mins

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