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How to Conduct a Human Factors Usability Validation for Medical Device Products

How to Conduct a Human Factors Usability Validation for Medical Device Products

Course Level: IntermediateOverview:Human Factors/ Usability is the analysis of how people interact ..

Date : 08th Feb 2023

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

Duration : 60 Mins

An Advanced Course on Lean Documents, Lean Configuration, and Document Control

An Advanced Course on Lean Documents, Lean Configuration, and Document Control

Overview:Just as a manufacturing process produces a product, controlled documents are the product o..

Date : 13th July 2022

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

Duration : 1 Hour 30 Mins

Risk-based Design Control - The New Paradigm for Medical Device Design

Risk-based Design Control - The New Paradigm for Medical Device Design

Overview: Risk management overarches projects associated with a particular product family, giv..

Date : 17th February 2022

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

Duration : 1 Hour 10 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

Risk Management for Medical Devices per ISO 14971:2019

Risk Management for Medical Devices per ISO 14971:2019

Overview: Risk management overarches projects associated with a particular product family, gi..

Date : 11th August 2021

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

Duration : 1 Hour 19 Mins

Software Validation Utilizing Principles of Lean Documents and Lean Configuration

Software Validation Utilizing Principles of Lean Documents and Lean Configuration

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

Date : 10th June 2021

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

Duration : 90 Mins

IEC 62304 for Medical Device Software - Is your Medical Device Software Out of Compliance?

IEC 62304 for Medical Device Software - Is your Medical Device Software Out of Compliance?

Overview:This course is essential for Medical Device companies interested in submitting software e..

Date : 23rd March 2021

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

Duration : 70 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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