Document Formatting, QC & Publishing Automation
From Content to Submission-Ready Documents
Managing Agency as well as company internal rules/guides manually can create significant effort and introduce avoidable risks. Regulatory, medical writing, CMC, labeling, publishing, and quality teams may spend hours checking formatting, validating references, reviewing tables, correcting hyperlinks, updating bookmarks, and ensuring documents comply with agency and internal rule books.
Document automation solutions connect formatting, quality control, and publishing into a streamlined, technology-enabled process.
Using REGai, organizations can automate repetitive document preparation and QC activities using rule-based automation, AI, or a hybrid approach. The result is a more consistent, traceable, and efficient path from working documents to submission-ready output.
70%+
Manual Efforts Reduced
65%
Lower Operating Costs
> 50%
Turn Around / Cycle Times Reduced
100%
Audit / Process Traceability
Automated Document Solutions
Connecting formatting, quality control, and publishing into a streamlined regulatory workflow.
Document Formatting Automation
Standardize Documents Against Regulatory and Corporate Requirements
Regulatory documents often involve hundreds of pages, multiple contributors, complex tables, figures, references, cross-references, and strict formatting requirements.
Manual formatting can result in inconsistent styles, incorrect pagination, broken links, misplaced content, table inconsistencies, and other technical issues that require repeated review and rework.
REGai’s Document Formatting Automation applies predefined regulatory and company internal rules to documents. The platform includes a library of more than 500 formatting rules and can automate common document-structure and layout activities.
Document Quality Control Automation
Move From Manual Inspection to Automated QC
Formatting is only one part of submission readiness. Regulatory documents must also be checked for consistency, completeness, structure, references, terminology, values, tables, and compliance with defined quality standards.
Manual QC across large regulatory documents is time-consuming and can make it difficult to achieve consistent results across teams and submission programs.
REGai’s QC Automation solutions provide a library of 600+ document checks covering areas such as formatting, grammar, tables, layouts, Tables of Contents, bookmarks, hyperlinks, consistency, and regulatory requirements.
Regulatory Publishing Automation
Transform Approved Documents Into Submission-Ready Output
Once content has been authored, formatted, and quality-checked, regulatory publishing brings the final pieces together.
Publishing teams often need to manage large volumes of Word and PDF files while validating document structure, hyperlinks, bookmarks, file naming, formatting, and eCTD-related requirements.
REGai’s publishing automation capabilities help streamline this final stage by applying automated validation and document-processing rules to prepare submission content efficiently. REGai supports publishing workflows using hundreds of automated rules for activities such as document formatting, tables, headers and footers, Tables of Contents, bookmarks, hyperlinks, file naming, and validation.
One Connected Approach to Regulatory Document Operations
Instead of treating formatting, QC, and publishing as separate manual activities, organizations can create a connected workflow that identifies issues earlier, automates repetitive corrections, and supports consistent regulatory output.
DDi brings these capabilities together through an automation-driven approach:
Prepare
Check
Fix
Publish
Track
This approach allows organizations to shift from manual document inspection and correction toward a more standardized and automated regulatory publishing process.
Ready to Transform Regulatory Document Operations?
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Frequently Asked Questions
Common questions about REGai Regulatory Operations document automation solutions.
What is REGai Regulatory Operations automation?
REGai is an automation platform designed for regulatory, medical writing, CMC, labeling, and publishing teams in life sciences. It connects document formatting, quality control (QC), and publishing into a streamlined workflow using rule-based automation and AI to produce submission-ready eCTD output.
What key business outcomes can organizations achieve using REGai?
Organizations using REGai experience:
- Over 70% reduction in manual document preparation effort
- 65% lower operating costs
- More than 50% decrease in turnaround and cycle times
- 100% auditability and end-to-end process traceability
How does REGai automate regulatory document formatting?
REGai standardizes complex documents against regulatory agency and internal corporate rule books. Utilizing a library of over 500 predefined formatting rules, it automatically corrects styles, pagination, tables, cross-references, and structural layouts across hundreds of pages.
What checks are included in REGai’s Document Quality Control (QC) Automation?
REGai provides a library of more than 600 automated document checks. These cover grammar, terminology, layout consistency, Tables of Contents (TOC), bookmarks, hyperlinks, table values, and regulatory compliance requirements.
How does REGai support regulatory publishing and eCTD preparation?
REGai automates final submission prep by managing Word and PDF files against eCTD requirements. It uses hundreds of automated processing rules to validate file naming, structure, headers/footers, bookmarks, and hyperlinks before submission.
What is the end-to-end workflow supported by DDi’s REGai platform?
DDi connects the entire regulatory document life cycle into a 5-step automated workflow: Prepare (apply formatting) → Check (run automated QC) → Fix (remediate identified issues) → Publish (validate for submission) → Track (maintain process traceability).
Let's talk about how DDi can help you