Vault Regulatory
Vault Regulatory
General Release 25R1GR
  • General Release 25R1GR
  • Limited Release 25R1.2LR
    • General
    • Submissions
    • Submissions Archive
    • Submissions Publishing
    • Registrations
  • Veeva Vault Release Notes
  • Veeva Vault Developer Portal
    • Veeva RIM Overview
    • RIM Application Settings & Configuration Options
    • Brexit Impact in RIM Vaults
    • RIM Maintenance
    • Application Chronology Reports
    • Configuring the Application Chronology Multi-Pass Report
    • Chronology Queries
    • Configuring Chronology Queries
    • Using Saved Views
    • Configuring Country Dependencies
    • Setting Up the RIM Reference Model
    • Automatic Record Creation in RIM Vaults
    • Configuring Constraints
    • Managing User Role Setup Object Types
    • Using the Hierarchy Viewer
    • Using the Legacy Hierarchy Viewer
    • Pulling Regulatory Objective Data to Submissions
    • Using Table of Contents Tokens
    • Viewing Publishing Progress
    • Using Dynamic Linking
    • Configuring Object Type Mapping
    • Email Processing (RIM)
    • About RIM Object Configurations
      • Using the RIM Document Classification Bot (RIM Bot)
      • Training Auto-Classification Models for RIM Bot
      • Evaluating RIM Bot Auto-Classification Models
      • About Active Dossiers
      • Active Dossier Configuration
      • Working with Active Dossiers
      • Managing Applications, Submissions, and Regulatory Objectives with the Submission Wizard
      • Submission Wizard Administration
    • Using CRF & Dataset Import
    • Setting Up CRF & Dataset Import
    • Working with Submission Validation Results
    • Pull Objective Data Configuration
      • Configuring Gateway Integration
      • About the EMA RMS Integration
      • Configuring Health Authority Interaction Extraction
      • Working with Health Authority Interactions
    • Veeva Submissions Overview
    • Configuring Report Level Publishing
    • Generating Form 2253
    • Configuring Form 2253 Generation for Submissions
    • Configuring a Workflow for Matched Documents
    • About SPL & XML Renditions
    • Configuring Cascading Review & Approval for Binder Content
      • Content Plan Filtering
      • Merging & Publishing Content Plans & Items
        • Using Global Content Plans
        • Dispatching & Synchronizing Content Plans
        • Configuring Global Content Plans
        • Configuring Content Plan Synchronization
      • Managing Content Plans with a Lifecycle
      • Configuring Cascading State Changes for Content Plans
      • Configuring Submission Content Plans
      • Configuring Report Level Content Plans
      • Copying Into Content Plans
      • Starting a Workflow in the Content Plan Hierarchy Viewer
      • Creating Content Plan Templates
      • Create a Document from Template for Content Plan Items
      • Using Submission Content Plans
      • Using Report Level Content Plans
      • Content Plan Lifecycle State Changes
      • Using the Content Plan Hierarchy Viewer
      • Using Keyboard Shortcuts in the Hierarchy Viewer
      • Configuring Atomic Security for Content Plan Actions
      • About the Progress Icon Field
      • Report Level Content Plan Validation Criteria
    • Veeva Submissions Archive Overview
    • Viewing Submissions in the Submissions Archive Viewer
    • About the New Submissions Archive Viewer
    • Enabling Correspondence Documents in Submissions Archive
    • About Submission Join Filters in Submissions Archive
    • Correcting Leaf Source File Paths
      • Preparing Submissions for Import
      • Importing Submissions
      • Submission Import Configuration
      • Importing Submissions with Vault File Manager for Windows
      • Configuring Submission Import with Vault File Manager
      • Exporting Submissions
      • Using Bulk Submission Export
    • Veeva Submissions Publishing Overview
    • Working with Submissions Publishing
    • Submitting to the FDA & EMA Electronic Submissions Gateways
    • Configuring Submissions Publishing
    • Configurable Validation Criteria
    • Managing Submission Administrative Information
    • Submission Administrative Information Configuration
    • Setting a Reference Leaf
      • Working with Hyperlinks in RIM Submissions Publishing
      • Working with Automated Linking & Link Evaluator
      • Configuring Automated Linking & Link Evaluator
      • Working with AU Regulatory Submissions
      • Working with CA Regulatory Submissions
      • Working with CH Regulatory Submissions
      • Working with EU Regulatory Submissions
      • Working with GCC Regulatory Submissions
      • Working with JO Regulatory Submissions
      • Working with JP Regulatory Submissions
      • Working with KR Regulatory Submissions
      • Working with TH Regulatory Submissions
      • Working with UA Regulatory Submissions
      • Working with US Regulatory Submissions
      • Working with WHO-PQT Regulatory Submissions
      • Working with ZA Regulatory Submissions
    • RIM Registrations Overview
    • Using the Affiliate Home Tab
    • Affiliate Home Tab Configurations
    • Pausing Vault Java SDK Record Triggers in RIM Registrations
    • About Activity Dependencies
    • Managing Registered Details
    • Configuring Manage Registered Details
    • Importing MedDRA Terminology
    • Label Concept & Deviation Tracking
    • Configuring Label Concept & Deviation Tracking
    • Registration Verification
    • Configuring Registration Verification
    • UPD Configuration
    • Viewing FHIR Messages
      • Generating UDI Data for EUDAMED
      • Configuration for Generating UDI Data
      • Using the UDI Submission Viewer
      • Configuring the UDI Submission Viewer
      • Bundling Activities & Regulatory Objectives
      • Splitting Regulatory Objectives
      • Splitting Activities
      • Configuring Bundling & Splitting
      • Bulk Creating Activities, Submissions & Regulatory Objectives
      • Bulk Creating & Managing Event Details
        • Bulk Creating Product Registrations
        • Bulk Creating Investigational Registrations
        • Bulk Creating Active Substance Registrations
        • Bulk Creating Manufacturing Site Registrations
        • Configuration for Bulk Creating Activities, Submissions & Regulatory Objectives
        • Configuration for Bulk Creating & Managing Event Details
        • Configuration for Bulk Creating Registrations
      • IDMP Configuration
      • Using the IDMP Viewer
      • Generating IDMP Data
      • About the Authorised Pharmaceutical Form & Registered Site Role Data Migrations
      • XEVMPD Data Review & Validation
      • XEVMPD Gateway Submission for Medicinal Products
      • XEVMPD Gateway Submission for Attachments
      • XEVMPD Bulk Update & Submission
      • XEVMPD Configuration
      • Generating eAF Output Reports
      • Configuring eAF Output Reports
      • Impact Assessment Reports
      • Setting Up Configurable Impact Assessment Reports
      • Setting Up Standard Impact Assessment Reports
      • Generating the Registration History Report
      • Registration History Report Configuration

Generating Form 2253 (RIM)

Note: This RIM Submissions feature is deprecated as of 22R3 (22R2.3). We recommend generating FDA 2253 Forms in a PromoMats Vault and CrossLinking to a RIM Vault via the RIM to PromoMats Vault Connection.

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Page last updated: Apr 21, 2025