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Laura A. Dixon

Updates to CMS Conditions of Participation and Reg

Live Webinar | Healthcare

Duration: 90 Minutes
Date: May 28, 2026 | , 01 : 00 PM EST 7 Days Left

John E Lincoln

US FDA Medical Device QSR (21 CFR 820) Quality Man

Live Webinar | Pharmaceutical

Duration: 90 Minutes
Date: May 29, 2026 | , 01 : 00 PM EST 8 Days Left

Mark Schwartz

Termination Pay - A Summary of State and Federal G

Live Webinar | Human Resources

Duration: 75 Minutes
Date: Jun 02, 2026 | , 01 : 00 PM EST 12 Days Left

Carolyn D. Riggins

Coaching vs. Corrective Action: How to Manage Perf

Live Webinar | Human Resources

Duration: 90 Minutes
Date: Jun 03, 2026 | , 01 : 00 PM EST 13 Days Left

Charles H. Paul

ChatGPT / AI for Project Management for FDA-Regulated Companies

Pharmaceutical

Duration: 60 Minutes |
From: May 07, 2026 - To: Dec 31, 2026

Lynn Anderanin

Medicare Telehealth Coverage in the 2026 Physician Fee Schedule Final Rule

Healthcare

Duration: 60 Minutes |
From: May 04, 2026 - To: Dec 31, 2026

Dr. Michael C. Redmond

CMS QAPI 2026: Strong Systems for Compliance and Quality Improvement

Healthcare

Duration: 60 Minutes |
From: Apr 30, 2026 - To: Dec 31, 2026

Suzanne Lucas

How to Document Employee Behavior: Protect Yourself and Lead with Confidence for Managers

Human Resources

Duration: 60 Minutes |
From: Apr 30, 2026 - To: Dec 31, 2026

Yesenia Servin

Credentialing and Enrollment: A Practical Guide to Revenue Cycle Collaboration 2026

Healthcare

Duration: 60 Minutes |
From: Apr 29, 2026 - To: Dec 31, 2026

Michael C Redmond

HIPAA Compliance Under Pressure: HHS Audit and Cybersecurity Priorities for 2026

Healthcare

Duration: 60 Minutes |
From: Apr 29, 2026 - To: Dec 31, 2026

Ginette Collazo

AI Errors May Be Impossible to Eliminate – What That Means for Its Use in the FDA

Pharmaceutical

Duration: 60 Minutes |
From: Apr 29, 2026 - To: Dec 31, 2026

Margie Faulk

EEOC Harassment Investigations: Practical Compliance and Documentation to Reduce Risk

Human Resources

Duration: 90 Minutes |
From: Apr 28, 2026 - To: Dec 31, 2026

John E Lincoln

Master Validation Plan for FDA cGMP Compliance

Pharmaceutical

Duration: 180 Minutes |
From: Apr 28, 2026 - To: Dec 31, 2026

Roger Cowan

GMP Environmental Monitoring for Pharmaceutical Clean Rooms

Pharmaceutical

Duration: 60 Minutes |
From: Apr 23, 2026 - To: Dec 31, 2026

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Updates to CMS Conditions of Participation and Reg

US FDA Medical Device QSR (21 CFR 820) Quality Man

Termination Pay - A Summary of State and Federal G

Coaching vs. Corrective Action: How to Manage Perf

ChatGPT / AI for Project Management for FDA-Regulated Companies

Medicare Telehealth Coverage in the 2026 Physician Fee Schedule Final Rule

CMS QAPI 2026: Strong Systems for Compliance and Quality Improvement

How to Document Employee Behavior: Protect Yourself and Lead with Confidence for Managers

Credentialing and Enrollment: A Practical Guide to Revenue Cycle Collaboration 2026

HIPAA Compliance Under Pressure: HHS Audit and Cybersecurity Priorities for 2026

AI Errors May Be Impossible to Eliminate – What That Means for Its Use in the FDA

EEOC Harassment Investigations: Practical Compliance and Documentation to Reduce Risk

Master Validation Plan for FDA cGMP Compliance

GMP Environmental Monitoring for Pharmaceutical Clean Rooms

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Updates to CMS Conditions of Participation and Reg

US FDA Medical Device QSR (21 CFR 820) Quality Man

Termination Pay - A Summary of State and Federal G

Coaching vs. Corrective Action: How to Manage Perf

ChatGPT / AI for Project Management for FDA-Regulated Companies

Medicare Telehealth Coverage in the 2026 Physician Fee Schedule Final Rule

CMS QAPI 2026: Strong Systems for Compliance and Quality Improvement

How to Document Employee Behavior: Protect Yourself and Lead with Confidence for Managers

Credentialing and Enrollment: A Practical Guide to Revenue Cycle Collaboration 2026

HIPAA Compliance Under Pressure: HHS Audit and Cybersecurity Priorities for 2026

AI Errors May Be Impossible to Eliminate – What That Means for Its Use in the FDA

EEOC Harassment Investigations: Practical Compliance and Documentation to Reduce Risk

Master Validation Plan for FDA cGMP Compliance

GMP Environmental Monitoring for Pharmaceutical Clean Rooms

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