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.




The 6 Most Common Problems in FDA Software Validation and Verification in 2026 -

The 6 Most Common Problems in FDA Software Validation and Verification in 2026 -

Overview: Software validation and verification remain common sources of compliance risk for FDA..

Date : 22nd July 2026

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

Duration : 75 Mins

CAPA Under QMSR: Root Cause, Risk, and Effectiveness Verification

CAPA Under QMSR: Root Cause, Risk, and Effectiveness Verification

Overview: CAPA is one of the most closely examined parts of a medical device quality system, ..

Date : 23rd July 2026

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

Duration : 75 Mins

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