Vault Quality
Vault Quality
General Release 26R1GR
  • General Release 26R1GR
  • Limited Release 26R1.2LR
    • General
    • QualityDocs
    • Vault Training
    • Station Manager
    • QMS
    • Product Surveillance
    • Validation Management
    • Batch Release
    • HACCP
  • Veeva Vault Release Notes
  • Veeva Vault Developer Portal
    • Quality Overview
    • Managing Departments
    • Managing Facilities
    • Managing Organizations
    • About the Quality Relationships Doc Info Panel
      • External Collaboration Overview
      • Quality External User Templates
    • QualityDocs Overview
    • Configuring QR Code Generation
    • Managing Regulatory Reference Requirements
      • Document Control Homepage
      • Setting Up the Document Control Homepage
      • Working with Document Change Requests
      • Working with Multi-Document Change Control
      • About Single-Document Change Control
      • Working with Single-Document Change Control
        • Configuring Document Change Requests
        • Configuring Multi-Document Change Control
        • Configuring Periodic Review
        • Mandatory Participants
      • Extensible Controlled Copy Configuration
      • Working with Extensible Controlled Copies
      • Distributing Legacy Controlled Copies
      • Using the QualityDocs Process Navigator
      • Configuring Process Navigator
      • Managing Visual Hierarchies
      • Working with Document Review & Approval External Collaborators
      • Configuring External Collaboration for Document Review & Approval
    • Veeva Training Overview
    • Using Veeva Station Manager
    • Veeva Station Manager Application Setup
    • Veeva Station Manager Configuration
    • Veeva Station Manager Custom URLs & QR Codes
    • Veeva Station Manager Document Categorization
    • Enterprise Mobility Management for Veeva Station Manager
    • QMS Overview
    • Managing Quality Event Data Models
    • Migrating Legacy Data to QMS
      • Configuring Quality Teams
      • Working with Quality Teams
    • Quality Relationship Automation
      • Using Quality Incidents
      • Configuring Quality Incidents
      • Using Quality Event Suggestions
      • Configuring Quality Event Suggestions
      • Using Change Action Paths & Steps
      • Configuring Change Action Paths & Steps
      • Working with Issue Escalation
      • Configuring Issue Escalation
      • Using External Notifications
      • Configuring External Notifications
      • Using External Response Collaboration
      • Configuring External Response Collaboration
      • Working with External Collaboration Checklists
      • Configuring External Collaboration for Checklists
      • Configuring External Collaboration Checklists with Follow-Ups & Additional Respondents
      • Working with Quality Automated Language Translations
      • Configuring Quality Automated Language Translations
      • Using Complaint Intake & Promote to Complaint
      • Configuring Complaint Intake & Promote to Complaint
      • Working with Complaint Email Ingestion
      • Configuring Complaint Email Ingestion
    • Configuring the Related Events Section
    • Configuring the Create Effectiveness Check Entry Action
    • Configuring the Sibling Check Related Record State Change Entry Action
    • Configuring the QMS Change Related Object Lifecycle State Job Entry Action
    • Configuring the Create Record from Template Action
    • Configuring the Set Permissions on Related Object Action
    • Configuring Record History
      • About the Record Check Interface
      • About the Recurrence Check Insights Page
      • Using Recurrence Check
      • Using Duplicate Check
      • Configuring Recurrence Check
      • Configuring Duplicate Check
    • Cycle Time Metrics
    • Related Record Configurations
    • Quality Document Generation
      • Using Annual Product Quality Reviews
      • Configuring Annual Product Quality Reviews
      • Using Quality Management Reviews
      • Configuring Quality Management Reviews
      • Using Periodic Safety Update Reports
      • Configuring Periodic Safety Update Reports
      • Assessing Adverse Event Reportability
      • Configuring Adverse Event Reportability
      • Working with Supplier Change Notifications
      • Working with External Supplier Collaborators
      • Configuring Supplier Change Notifications
    • Continuous Improvements & Standalone CAPAs
      • Using 5 Whys Analysis
      • Working with External Investigation Collaborators
      • Configuring Root Cause Analysis
      • Risk Assessments
      • Working with Supplier Risk Assessments
      • Risk Builder
      • Risk Management
      • Using Periodic Risk Review
      • Configuring Periodic Risk Review
      • Configuring Assessments
      • Configuring Supplier Risk Assessments
      • Working with Audit Room
      • About the Audit Room Page
      • Configuring Audit Room
      • Working with Audit Programs
      • Working with External Audit Collaborators
      • Managing Auditor Profiles, Roles, & Qualification Criteria
      • Auditor Qualification
      • Checklists for Audits
      • Configuring Audit Program Planning
      • Configuring Auditor Profiles & Qualifications
      • Providing a Reason for Change
      • Configuring Reason for Change
      • Working with Field Corrective Actions
      • Configuring Field Corrective Actions
      • Using the Complaint Agent
      • Configuring the Complaint Agent
      • Using the Deviation Agent
      • Configuring the Deviation Agent
    • Product Surveillance Overview
    • Using MedTech Complaint Adverse Event Reporting
    • Configuring Adverse Event Reporting
    • Configuring FDA Gateway Integration
    • Submitting eMDR XML Documents to the FDA ESG
    • Validation Management Overview
    • Setting Up Validation Management
    • Configuring Family Validation
    • Configuring Test Step Additional Prompts
    • Printable View Administration
    • Managing Requirements
    • Managing Templates
    • Managing Periodic Reviews
    • Authoring Test Scripts
    • Dry Running Test Scripts
    • Executing & Reviewing Test Scripts
    • Reviewing Test Protocols
      • Configuring Test Step Additional Prompts
    • Batch Release Overview
    • About the Batch Release Execution Page
    • Setting Up Batch Release
    • About Batch Genealogy
    • About Batch Disposition Checks
      • Working with Batch Release Roles
      • Configuring Batch Release Roles
    • HACCP Overview
    • Working with HACCP Plans
    • Working with the HACCP Flow Diagram
    • Performing Hazard Analysis & Defining Control Measures
    • Translating HACCP Plans
    • Configuring HACCP
    • Configuring HACCP Plan Translation

Configuring Additional Test Step Prompts

Test Step Additional Prompts are available in the Test Authoring Interface and the Text Execution Interface for setup and execution steps. This video demonstrates how to configure test step additional prompts.

Learn More

The following links provide additional information and resources about this topic:

  • Configuring Test Step Additional Prompts (Validation Management)
  • Authoring Test Scripts (Validation Management)
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Page last updated: Apr 29, 2026