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The Seal Platform
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  • Logging in & System Requirements
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  • Moving to Seal
    • Migration
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  • Manage
    • Where do I start?
    • Creating Types
      • Documents
      • Work Done
      • Files
        • Extracting Fields with AI
      • Scripts
        • Writing Scripts with the Seal Module
        • Script Action Buttons
      • Charts
      • Converting Between Types
    • Adding Content and Fields
      • Computed Titles
      • Formatting Text
      • Formulas
      • Numbered Lists
      • Setting Assignees
      • Setting Out-of-Specifications
      • Setting Review Requirements
      • Submission Tables
    • Executing Types: Test Instances
    • Work Instructions
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    • Active Versions
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  • Operate
    • Where do I start?
    • Re-executing Instances
    • Reviewing
  • MISC
    • Glossary
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    • Search Page and Saved Views
    • User Permissions and Roles
    • Tags
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    • Seal Changelog
  • Video Guides
    • Creating Templates
    • Creating and Reviewing Instances
    • Sending and Completing Trainings
  • Validation
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    • What is needed from my end for validation?
    • How is my system validated?
      • Baseline Validation
      • Configuration Validation
      • Compliance Validation
      • What about IQ, OQ, or PQ?
      • Automatic Revalidation
        • Change Controls
      • How do I know if my system is compliant to a standard?
        • Setting up your System
        • Performing Compliance Validation
    • GxP Validation for enterprise customers
    • Can I download a Validation Report?
      • Software Functionality Verification
    • Common Validation FAQs
  • Product Quality
    • Seal's Guarantee of Quality
    • Product Development Lifecycle
    • Platform Operation Tests
    • Incident Procedure
  • IT & Security Policies
    • Seal's Tech Stack
    • Data Storage and Security
    • Cloud Servers vs On-Premises File Servers
    • Data Backup and Disaster Recovery
    • Disaster Recovery Plan
    • Handling Confidential Data
    • Common IT FAQs
  • Regulatory Standards
    • 21 CFR Part 11
    • EU Volume 4 Annex 11
    • ISO 13485 Medical Devices
    • Clinical Laboratory Improvement Amendments (CLIA)
  • Support
    • Contact us
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  1. MISC

Tags

Last updated 1 month ago

Tags are 'labels' that can be added to any object. Multiple tags can be added to an object.

Tags are useful for grouping similar objects together, and can be easily searchable using tag: in the search bar.

Note that tags are not classed as entity data - this means they can be changed without needing to create new drafts of any published entities.

Navigate to the settings page to manage all tags within your organisation.