Structured Content AI

Meet Your New Authoring Assistant

Our ComplianceAuthor® AI structured content platform empowers global teams to create, manage and deploy structured content across the enterprise. Automate manual tasks, streamline workflows, and deliver submission-ready output in half the time.

Train AI on Your Regulatory Content

Use AI pre-trained on life science content to instantly identify relevant documents, unlock insights, transform unstructured data, and author compliant output.

Glemser Compliance Author
Glemser Compliance Author

Reuse Compliant Components for Any Output

Create and deploy structured content components across the globe. Make a change once, and see it automatically flow to compliant downstream output.

Scale Your Authoring Process Safely

Ingest, index, contextualize and componentize your entire enterprise content corpus, and deploy it at scale in any format you need.
Glemser Compliance Author

Structured Content AI

Add Generative AI to Any  Authoring Workflow

Apply a powerful, AI-powered toolset to use cases across global labeling, clinical labeling, test specifications for CMC, and more. And all without compromising compliance or safety.

Key Benefits

Streamline Structured Content Management

Our unique and meticulous approach addresses the most intricate nuances of the pharmaceutical industry, so your team is empowered to tackle operational challenges.
0 %
Reduction in Labeling Timeline
0 %
Cost Savings​


Work Within Familiar Systems

ComplianceAuthor® AI tools can be accessed directly within applications like Microsoft Word® and Quark™, and integrate natively with solutions from Veeva, SAP, SharePoint, Oracle, and Documentum. Every common file type is supported. We don’t ask you to replace your core business systems – we’re here to add functionality, capabilities, and speed.

Glemser Integrations