Word add-in for regulatory affairs

AI Word add-in for medical device regulatory documents

Draft, review, translate, and improve CER, CEP, GSPR, and regulatory submission content directly inside Microsoft Word with RAQB.
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Built for Word-based regulatory workflows

RAQB helps teams keep regulatory writing, evidence references, and document revisions in the place where work already happens.

Draft structured regulatory sections

Generate first-pass CER, CEP, GSPR, and submission-ready sections from product context, templates, and reviewer instructions.

Review language against evidence

Ask questions about pasted references, uploaded material, and knowledge base content while keeping the draft open in Word.

Translate and refine document text

Rewrite, shorten, translate, or clarify selected text without moving content through separate tools or manual copy-paste loops.

Questions teams ask before adopting RAQB

Practical answers for regulatory affairs, quality, clinical, and product teams evaluating RAQB.

Is this a replacement for regulatory review?

No. RAQB supports drafting, organization, and review workflows. Final regulatory decisions remain with qualified subject matter experts.

Which documents does the Word add-in support?

The strongest fit is CER, CEP, GSPR, IFU, clinical summaries, evidence summaries, and other Word-based regulatory affairs documents.

Can teams use their own templates?

Yes. RAQB is designed around templates and structured document workflows, including marketplace and team-managed templates.

Does it work with existing Word files?

Yes. The add-in workflow is built for teams that already author and revise regulatory documents in Microsoft Word.

Start with templates, pricing, or a direct conversation.

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