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Structured Content Authoring

Create documents with customizable editable fields and pre-approved content to reduce compliance risk.

Solution by Papercurve
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Overview

Structured Content Authoring is a document creation capability within Papercurve that allows users to build documents using customizable editable fields and pre-approved content blocks. It is designed for organizations that need to control what text can be modified in distributed documents, particularly in regulated or compliance-sensitive environments where unauthorized changes carry risk.

The tool supports document types built from existing Microsoft Word, PowerPoint, and Excel files, avoiding proprietary vendor formats and giving teams full design control using familiar tools.

Core Capabilities

  • Distributes agreements and contracts with selected editable fields, limiting changes to only designated areas of the document.
  • Allows only structured, pre-authorized content to be generated within a document, reducing the risk of unauthorized modifications.
  • Supports repurposing of previously created and approved content in new documents, speeding up the content creation process.
  • Stores documents containing editable fields or structured content in a central, secure location for reuse and easy access.
  • Automatically detects placeholder locations using the {{double brackets}} convention, identifying editable fields within uploaded documents.

Content Management and Governance

  • Centralizes approved content in a single location, making it easier to update content and onboard new users.
  • Enables risk-free document creation by restricting authoring to pre-authorized phrases and approved content blocks.
  • Supports compliance review processes by maintaining structured, auditable document records.

Format and Integration Support

  • Compatible with Microsoft Word, PowerPoint, and Excel file formats.
  • Does not require migration to vendor-specific formats, preserving existing design and layout choices.

Papercurve is based in Toronto, Canada, and offers additional resources including integrations, data security documentation, and case studies. Organizations looking to streamline compliance review and maintain compliant document records can explore the platform through a discovery call.

Meta

Domain
Commercial & Medical Affairs
Subdomain
Medical Affairs Operations
Software type(s)
Workflow Automation
Deployment type(s)
Cloud / SaaS
Industry vertical(s)
PharmaBiotechMedical Devices
Development stage(s)
ClinicalPost-Market & RWE
Target user(s)
QA / Regulatory AffairsMedical Affairs ProfessionalCommercial / Market Access
Compliance standard(s)
GxP