Veeva Safety Newsletter
Safety Innovation and
Industry News
Highlighting key industry insights, technology innovation,
and biopharmas advancing safety.
Newsletters
Issue 8
Connected Systems: Fastest Path to an Inspection-Ready PSMF
Explore how pharmacovigilance (PV) teams can use connected regulatory and safety systems to reduce manual updates and increase PSMF accuracy.
Issue 7
Faster and Easier Literature Review to Case Intake
Literature review is a significant source of individual safety case reports (ICSRs). Learn how automation and an integrated safety system greatly reduces manual effort, as well as compliance and patient safety risks.
Issue 6
Get Ready for FDA E2B(R3): What PV Teams Need to Know
Understand FDA E2B(R3) reporting requirement for serious and unexpected suspected adverse reactions (SUSARs) and what PV teams need to do to prepare for the upcoming deadline.
Issue 5
Automate Safety Letter Distribution: 80% Faster and 50% Less Effort
How safety letter distribution automates delivery of critical safety information to investigators and regulators with speed, efficiency, and quality.
Issue 4
Reduce Reconciliation of Clinical Serious Adverse Events (SAE)
Spotlight on the Safety-EDC Connection and how it automates the flow of serious adverse event (SAEs) records from data management teams to the safety inbox and reduces reconciliation.
Issue 3
Bring Safety In-house for Better Oversight, Simplified Operational Reporting, and CRO Flexibility
How to achieve greater CRO collaboration and better pharmacovigilance (PV) oversight with easier operational reporting.
Issue 2
Reduce Case Rework and Increase Data Quality by Improving Case Processing Workflow
The importance of quality control (QC) checklists in an end-to-end case processing workflow.
Issue 1
Growing Risk Management Findings: How to Get Ahead and Improve Compliance
Learn why risk management is a top source of safety inspection findings and how to enhance your approach to global risk management.