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Mandatory Paid Sick Leave  Breaking Through the Quagmire and Quandary of Compliance

Mandatory Paid Sick Leave Breaking Through the Quagmire and Quandary of Compliance

Overview: As of 2024, eighteen states plus the District of Columbia have mandated that employ..

Date : 23rd April 2024

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

Duration : 90 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

Risk-Based Approach to Validating IT Infrastructure Used for FDA-Regulated Systems

Risk-Based Approach to Validating IT Infrastructure Used for FDA-Regulated Systems

Overview: For over three decades, the FDA has regulated computer system validation (CSV) acro..

Date : 25th March 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

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

How to Conduct an ACH Risk Assessment and Develop an Effective Risk Management Program

How to Conduct an ACH Risk Assessment and Develop an Effective Risk Management Program

Overview:In today's digital payment landscape, Financial Institutions, Third-Party Service Provide..

Date : 22nd February 2024

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

Duration : 90 Mins

Employee Handbook Requirements for 2024. Includes Updated Federal, State and Local Regulations as well as Multi-State Regulations!

Employee Handbook Requirements for 2024. Includes Updated Federal, State and Local Regulations as well as Multi-State Regulations!

Overview: If there’s ever a time to rethink your employee handbook, it’s now. The wave of cha..

Date : 30th January 2024

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

Duration : 90 Mins

FDA Regulation of Artificial Intelligence/ Machine Learning Software following the new draft Guidance

FDA Regulation of Artificial Intelligence/ Machine Learning Software following the new draft Guidance

Overview: Artificial Intelligence (AI) and Machine Learning (ML) are fast becoming game-change..

Date : 24th October 2023

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

Duration : 75 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 digital age, where data integrity and privacy are more critical than eve..

Date : 12th October 2023

Time : This Event is Over

Duration : 90 Mins

Complying with the NEW I-9 and E-Verify Regulations - The Iceman Cometh

Complying with the NEW I-9 and E-Verify Regulations - The Iceman Cometh

Overview: On August 1, 2023, the landscape of employment eligibility verification changed dra..

Date : 19th September 2023

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

Duration : 90 Mins

510K Submission Process for Medical Devices

510K Submission Process for Medical Devices

Overview: There are three types of 510(k) submissions that can be submitted – Traditional, Spec..

Date : 25th August 2023

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

Duration : 75 Mins

Nacha Rules 2022-23: Key Changes, Compliance & Impact Analysis

Nacha Rules 2022-23: Key Changes, Compliance & Impact Analysis

Overview:The Automated Clearing House (ACH) Network serves as the backbone of electronic money mov..

Date : 22nd August 2023

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

Duration : 75 Mins

Mastering Mobile App Validation in FDA-Regulated Environments

Mastering Mobile App Validation in FDA-Regulated Environments

Overview: In this webinar, we will delve into the critical aspects of applying computer syste..

Date : 26th May 2023

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

Duration : 90 Mins

FDA Regulation of Artificial Intelligence/ Machine Learning - New FDA Guidance

FDA Regulation of Artificial Intelligence/ Machine Learning - New FDA Guidance

Overview:Explore how AI/ML is transforming medicine by making diagnosis and treatment more accessibl..

Date : 27th April 2023

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

Duration : 75 Mins

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