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The FMLA in 2026: Employer Compliance, Intermittent Leave, and Managing Suspected Abuse
Overview:Managing FMLA leave in 2026 is rarely as simple as approving 12 weeks of unpaid leave and ..
Date : 10th June 2026
Time : This Event is Over and the Recorded Content is Available
Duration : 75 Mins
Medical Device Cybersecurity Following FDA’s 2026 Premarket Guidance
Overview Cybersecurity is now a central part of FDA’s review expectations for many connected, ..
Date : 28th May 2026
Time : This Event is Over and the Recorded Content is Available
Duration : 60 Mins
HR Documentation: How Can HR Professionals and Supervisors Create Litigation-Proof Decisions in 2026
Overview: Employee documentation continues to be one of the most sensitive and mishandled area..
Date : 31st March 2026
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
Supplier Selection and Contract Manufacturer Qualification Under FDA QMSR
Overview: FDA’s QMSR places renewed emphasis on the way medical device companies evaluate, se..
Date : 24th March 2026
Time : This Event is Over and the Recorded Content is Available
Duration : 75 Mins
Employers Should Prepare for Immigration Raids in 2026! This Means More I-9 Audits for Employers by ICE
Overview: Worksite immigration enforcement can turn into an operational crisis faster than mos..
Date : 26th February 2026
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
ISO 13485:2016 Utilizing Principles of Lean Documents and Lean Configuration
Overview: Medical device and life science organizations are expected to maintain a Quality Ma..
Date : 20th February 2026
Time : This Event is Over and the Recorded Content is Available
Duration : 75 Mins
2026 Nacha Rules Changes (Part 1): Fraud Monitoring & Ops Bulletins
Overview: The ACH Network runs on precision—formats, timing, authorizations, monitoring expec..
Date : January 28, 2026
Time : This Event is Over and the Recorded Content is Available
Duration : 120 Mins
FDA’s QMSR is Coming: Practical Readiness for Quality Teams
Overview: With the FDA’s Quality Management System Regulation (QMSR) taking effect in February..
Date : 21st January 2026
Time : This Event is Over and the Recorded Content is Available
Duration : 60 Mins
Multi-State Payroll Tax Compliance 2025: Managing Remote Work, Reciprocity & SUI Challenges
Overview: Running payroll across multiple jurisdictions is no longer an edge case—it’s the wee..
Date : 18th November 2025
Time : This Event is Over and the Recorded Content is Available
Duration : 60 Mins
Exempt vs, Non-exempt and how the FLSA Defines Each
Overview: The Fair Labor Standards Act (FLSA) continues to be one of the most critical and co..
Date : 03rd November 2025
Time : This Event is Over and the Recorded Content is Available
Duration : 60 Mins
Project Management for CSV in FDA-Regulated Environments (CSA, GAMP®5 2nd Ed.) — with a Brief AI/ChatGPT Overview for PM Support
Overview: Computer System Validation (CSV) has underpinned FDA compliance in regulated industr..
Date : 30th October 2025
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
I-9 Audits & ICE Workplace Raids: What Employers Must Do Now to Stay Compliant
Overview: With the Trump administration now in office, immigration enforcement has swiftly es..
Date : 22nd July 2025
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
FDA Human Factors Usability Guidance | ISO 62366 & Draft Update Explained
Overview: Human Factors/Usability studies are essential in ensuring that medical devices are ..
Date : 29th May 2025
Time : This Event is Over and the Recorded Content is Available
Duration : 75 Minutes
HR Documentation: How Can HR Professionals and Supervisors Create Litigation Proof Decisions in 2025
Overview: In the fast-paced world of human resources, documentation isn't just about keeping ..
Date : 25th April 2025
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
Excel Spreadsheet in FDA Regulated Environment - Ensuring Data Integrity and 21 CFR Part 11 Compliance in 2025
Overview:The use of Excel in FDA-regulated environments extends beyond basic data organization and a..
Date : 11th April 2025
Time : This Event is Over
Duration : 90 Mins