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Scrutinizing Test Method Validation (TMV) to Verify the Performance of a Medical Device

Scrutinizing Test Method Validation (TMV) to Verify the Performance of a Medical Device

Overview: Test Method Validation (TMV) is a critical yet often misunderstood requirement in t..

Date : 21st October 2024

Time : This Event is Over and the Recorded Content is Available

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 : This Event is Over and the Recorded Content is Available

Duration : 75 Mins

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

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

Overview: All life science businesses are required to maintain their Quality Management Syste..

Date : 21st September 2021

Time : This Event is Over and the Recorded Copy is Available

Duration : 1 Hour 30 Mins

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