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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 : This Event is Over and the Recorded Content is Available

Duration : 90 Mins

The 6 Most Common Problems in FDA Software Validation and Verification in 2024

The 6 Most Common Problems in FDA Software Validation and Verification in 2024

Overview: Professionals working with FDA-regulated software face numerous challenges when it c..

Date : 18th July 2024

Time : This Event is Over

Duration : 75 Mins

Mastering Mobile App & Medical Device Software Validation and Cybersecurity in FDA-Regulated Environments

Mastering Mobile App & Medical Device Software Validation and Cybersecurity in FDA-Regulated Environments

10 Minutes excerpt from the recorded event for your review: Read the LinkedIn Article: Lin..

Date : 28th June 2024

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

Duration : 90 Mins

Medical Device Software Verification and Validation Following FDA 2023 Guidance and ISO 62304

Medical Device Software Verification and Validation Following FDA 2023 Guidance and ISO 62304

Overview: In the fast-evolving field of medical technology, ensuring the safety and efficacy ..

Date : 28th May 2024

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

Duration : 60 Mins

GAMP®5, 2nd Edition & FDA's CSA Guidance - Aligning Validation Practices

GAMP®5, 2nd Edition & FDA's CSA Guidance - Aligning Validation Practices

Overview The landscape of computer system validation is undergoing a transformative shift wit..

Date : 30th April 2024

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

Duration : 90 Mins

Computer Software Assurance: Risk-Based Validation With Time-Saving Templates

Computer Software Assurance: Risk-Based Validation With Time-Saving Templates

Overview:This webinar describes exactly what is required for compliance with Part 11 and the Europe..

Date : 30th January 2023

Time : This Event is Over

Duration : 90 Mins

Medical Device Software Validation Meeting FDA Regulations

Medical Device Software Validation Meeting FDA Regulations

Overview: Testing software to prove that it works and has no bugs is not sufficient to obtain ..

Date : 25th October 2022

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

Duration : 75 Mins

The 6 Most Common Problems in FDA Software Validation and Verification - What to Know?

The 6 Most Common Problems in FDA Software Validation and Verification - What to Know?

Overview:This webinar describes the validation planning process with particular emphasis on avoidin..

Date : 14th July 2022

Time : This Event is Over

Duration : 90 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

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