LearnGxP Releases

Last updated: May 21, 2026

May 2026

Scheduled for release on May 26, 2026

New & Updated Courses

NameNewRedesign
CLC-101 Codes of Conduct
EHS-123 Electrical Safety
ELM-121 Risk-Based Equipment Qualification
ELM-135 MDSAP Essentials: A Global Regulatory Roadmap
ELM-224 The GxP Road Map: From Pipeline to Patient
EQT-002 Autoclaves

Retired Courses

Note Training Requirements for retired Veeva LearnGxP courses are not automatically retired in your Vault. You will need to obsolete the course manually.
NameRetiredNotes
ELM-321 EU-MDR - Chapter V - Classification and Conformity AssessmentCombined with ELM-320 EU Medical Device Regulation
ELM-322 EU-MDR - Chapter VI - Clinical Evaluation and Clinical InvestigationsCombined with ELM-320 EU Medical Device Regulation
ELM-323 EU-MDR - Chapter VII - Post Market Surveillance, Vigilance and Market SurveillanceCombined with ELM-320 EU Medical Device Regulation

April 2026

Scheduled for release on April 28, 2026

New & Updated Courses

NameNewRedesign
ELM-154 CSA and Data Integrity: Assuring ALCOA+
ELM-166B CSA: Leveraging Supplier Assurance
EQT-003 Balances and Scales
MLV-003 The Principles of Production Operations in a GMP Environment
MLV-008 Good Documentation Practices - Signatures
MLV-009 Good Documentation Practices - Scrap Paper and Sticky Notes
MLV-010 Good Documentation Practices - How to Make Corrections

Retired Courses

No courses were retired this month. See upcoming retirement notifications.

March 2026

Scheduled for release on March 31, 2026

New & Updated Courses

NameNewRedesign
ELM-124 Audit Execution
ELM-133 Integrating Assurance into the Software Life Cycle
ELM-814 Quality Management System Regulation (QSMR) and Global Harmonization
MLV-007 Good Documentation Practices - Time Format

Retired Courses

No courses were retired this month. See upcoming retirement notifications.

February 2026

Scheduled for release on February 24, 2026

New & Updated Courses

NameNewRedesign
CCL-129 Advertising and Promotion
ELM-123 Risk-Based Audit Planning and Preparation
ELM-320 EU Medical Device Regulation
ELM-959 Inspection Readiness for GCP - Responding to GCP Inspections
ELM-998 Clinical Trial Safety Reporting
MLV-006 Good Documentation Practices - Date Format
MLV-023 What are CAPAs?
MLV-024 What is Quality Risk Management (QRM)?

Retired Courses

No courses were retired this month. See upcoming retirement notifications.

January 2026

Scheduled for release on January 27, 2026

New & Updated Courses

NameNewRedesign
CCL-127 False Claims Act
ELM-111 CSV Through The Lens of CSA
ELM-162 CSA: Applying a Risk-Benefit Approach
ELM-265 The Fundamentals of GCP Deviations
ELM-266 The Fundamentals of GCP Corrective and Preventive Actions
ELM-348 In Vitro Diagnostic Medical Devices Regulation
ELM-989 Data Integrity Refresher 2026
ELM-990 Good Manufacturing Practices Refresher 2026
ELM-991 Good Clinical Practice Refresher 2026
ELM-992 Good Laboratory Practice Refresher 2026
ELM-993 Good Pharmacovigilance Practice Refresher 2026
ELM-994 Quality Management System Refresher 2026
ELM-995 GxP Hot Topics: Human Error Prevention Refresher 2026
ELM-996 ICH E6 R3 Appendices
ELM-999 Investigator Oversight of Clinical Trials
MLV-001 What are Good Manufacturing Practices (GMP)?
MLV-002 The Importance of GMP Compliance
MLV-004 The Importance of Good Documentation Practices
MLV-005 Core Requirements of Good Documentation Practices
MLV-016 What is Drug Contamination?
MLV-019 Sources of Contamination in a GxP Environment
MLV-021 Why are Regulatory Inspections So Critical?
MLV-046 Access Control
MLV-068 Importance of Timely Closures of Deviations
MLV-097 Product Contamination in the Consumer Healthcare Industry

Retired Courses

No courses were retired this month. See upcoming retirement notifications.