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Clinical Trial Systems: Trial Master File (TMF) and eTMF, & FDA’s Recent Draft Guidance for Electronic Records/Signatures Used in Clinical Trials
Overview: Organizations involved in the conduct of human clinical trials must meet rigorous re..
Date : 30th September 2025
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
How to Manage the Legal Landmine of the FMLA, ADA and Workers Compensation in the Workplace!
Overview: Understanding how to navigate the Americans with Disabilities Act (ADA) is a legal n..
Date : 23rd September 2025
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
Employee Expense Reimbursements: IRS Rules, Accountable Plans, Per Diems & OBBB Updates
Overview: Employee expense reimbursements may seem straightforward, but when handled incorrect..
Date : 15th September 2025
Time : This Event is Over and the Recorded Content is Available
Duration : 75 Mins
Validation of FDA-Regulated Systems with AI, ML & LLMs (ChatGPT)
Overview: Life science industries — including pharmaceutical, medical device, biotechnology, ..
Date : 11th September 2025
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
Business Process Mapping – How to Prepare a Detailed System & Data Roadmap for a Clinical Trial Regulated by FDA
Overview: Conducting human clinical trials requires strict adherence to government regulatory ..
Date : 30th October, 2024
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
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
Protect Your Workplace: Comply with the EEOC's New Harassment Guidance
10 Minutes excerpt from the recorded event for your review: Read the LinkedIn Article: Lin..
Date : 11th September 2024
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
Excel Spreadsheet in FDA Regulated Environment in 2023
Overview:The use of Excel in FDA-regulated environments goes beyond typical data organization and an..
Date : 28th September 2023
Time : This Event is Over
Duration : 90 Mins
Understanding the DOL's Proposed Overtime Salary Changes: What Employers Need to Know
Overview: On August 30, 2023, the U.S. Department of Labor (DOL) issued a significant proposa..
Date : 28th September 2023
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
Overview:Whether you're a Financial Institution, Third-Party Service Provider (TPSP), or Third-Par..
Date : 27th September 2023
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
Data Integrity and Data Governance for Computer Systems Regulated by FDA
Overview:Navigating the FDA's guidelines on computer system validation is no simple task, particul..
Date : 26th September 2023
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
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
NEW Nacha Rule – Third-Party Sender (TPS) Roles and Responsibilities
Overview:Recent updates to the Nacha Operating Rules are further clarifying the Roles and Responsibi..
Date : 30th September 2022
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
Unemployment Insurance – 2022 - 2023 Critical Issues
Overview: Unlike other human resource management issues, unemployment insurance (UI) managemen..
Date : 28th September 2022
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
Data Integrity and Governance for Computer Systems Regulated by FDA
Overview:The Webinar will focus on the importance of ensuring that the validation of an FDA-regulate..
Date : 27th September 2022
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins