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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

Human Factors/ Usability Studies following ISO 62366 , the FDA Guidance and the new FDA Draft Guidance

Human Factors/ Usability Studies following ISO 62366 , the FDA Guidance and the new FDA Draft Guidance

Overview: Human Factors/Usability studies are essential in ensuring that medical devices are ..

Date : 25th June 2024

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

Duration : 75 Mins

Multi-State Payroll Tax Compliance - June 2024

Multi-State Payroll Tax Compliance - June 2024

Overview: Navigating the complexities of multi-state payroll tax compliance can be a daunting ..

Date : 10th June 2024

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

Duration : 60 Mins

The Dos and Donts of Conducting Employee Criminal Background Checks: Staying Compliant with Regulations

The Dos and Donts of Conducting Employee Criminal Background Checks: Staying Compliant with Regulations

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

Date : 07th June 2024

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

Duration : 90 Mins

Best Practices for Auditing a Vendor of Computer Systems Regulated by FDA

Best Practices for Auditing a Vendor of Computer Systems Regulated by FDA

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

Date : 30th May 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

Multi-State Payroll Tax Compliance in 2024 - Navigating Complexities

Multi-State Payroll Tax Compliance in 2024 - Navigating Complexities

Overview In the dynamic and interconnected business environment of 2024, multi-state payroll ..

Date : 17th April 2024

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

Duration : 60 Mins

I-9 Compliance 2024: Corrections, Audits, and Best Practices

I-9 Compliance 2024: Corrections, Audits, and Best Practices

Overview In 2024, employers and HR professionals are navigating the complexities introduced b..

Date : 03rd April 2024

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

Duration : 90 Mins

Data Integrity and Privacy - Compliance with 21 CFR Part 11, SaaS/Cloud, EU GDPR-

Data Integrity and Privacy - Compliance with 21 CFR Part 11, SaaS/Cloud, EU GDPR-

Overview: In today's rapidly evolving life sciences landscape, ensuring data integrity and pr..

Date : 21st March 2024

Time : This Event is Over

Duration : 90 Mins

Nacha Rule – Third-Party Sender (TPS) Roles and Responsibilities - What to Know

Nacha Rule – Third-Party Sender (TPS) Roles and Responsibilities - What to Know

Overview: In 2022, Nacha implemented significant updates to its Operating Rules to enhance cl..

Date : 20th March 2024

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

Duration : 90 Mins

March 2024 Deadline: Understanding DOL's New Independent Contractor Classification Rule

March 2024 Deadline: Understanding DOL's New Independent Contractor Classification Rule

Overview: The upcoming 2024 Independent Contractor Rule by the U.S. Department of Labor (DOL) ..

Date : 29th February 2024

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

Duration : 90 Mins

Risk Management for ML medical devices following BS/AAMI 34971:2023 and ISO 14971

Risk Management for ML medical devices following BS/AAMI 34971:2023 and ISO 14971

Overview: FDA has always prioritized the risk management of medical devices, adhering to its ..

Date : 27th February 2024

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

Duration : 60 Mins

Validation of FDA-Regulated Systems that Incorporate Artificial Intelligence (AI) and Machine Learning (ML)

Validation of FDA-Regulated Systems that Incorporate Artificial Intelligence (AI) and Machine Learning (ML)

Overview: As the life sciences industry, encompassing pharmaceuticals, medical devices, biote..

Date : 23rd February 2024

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

Duration : 90 Mins

Excel Spreadsheets - Step-By-Step Instructions for Ensuring Data Integrity

Excel Spreadsheets - Step-By-Step Instructions for Ensuring Data Integrity

Overview:The use of Excel in FDA-regulated environments extends beyond basic data organization and..

Date : 29th January 2024

Time : This Event is Over

Duration : 90 Mins

Medical Device Cybersecurity following September 2023 FDA Premarket Guidance

Medical Device Cybersecurity following September 2023 FDA Premarket Guidance

Overview: This webinar will cover FDA's evolving position on medical device cybersecurity. The..

Date : 29th November 2023

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

Duration : 75 Mins

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