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Component-based structured content. Simplified by AI.

Streamline the way you draft and manage your most critical regulatory documentation with Glemser –structured content AI tools and IT solutions for pharma.

Component-based structured content. Simplified by AI
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 generate submission-ready output in half the time.

Train AI on your regulatory content

Leverage components to author and update faster, and then publish to many outputs.

Reuse compliant components
for any output

Create and deploy structured content components across the globe. Make a change once, and gain insights to determine the next best action.

Scale your authoring
process safely

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

scalability
USE CASES

Turbocharge authoring 
with generative AI

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

Global Labeling

Reduce the time to author and change product labels by 50%, from company core data sheets to local labels.

Clinical Labeling

Allocate resources properly and reduce errors and risks to increase overall profitability.

CMC Dossiers

Engineer superior, controlled components that sustain compliance and improve patient safety globally.

Translations

Translate content for your specific use case so it meets both language and regulatory requirements.

Key Benefits

Streamline structured content management

Our proven approach behind your firewall uses AI with a life sciences language model to automate the most cumbersome parts of your workflow, so your team is empowered to tackle operational challenges.

50%

Reduction in labeling
timeline

30%

Cost savings

50%

Reduction in labeling
timeline

30%

Cost savings

Shrink the average
labeling timeline

Enable automated data extraction and compare content against applicable regulations for an optimized workflow.

Reduce
extraneous costs

Enable automated data extraction and compare content against applicable regulations for an optimized workflow.

Boost quality &
compliance

Enable automated data extraction and compare content against applicable regulations for an optimized workflow.

Quotes

What teams say about Glemser

"This is an opportunity to significantly enhance our speed and quality – both critical for the pharma supply chain. I would be keen at some point to understand how to link the Compliance Author system to other things within our supply chain. I do believe we can use the technology and capability of the Glemser team in other areas of the business."

Director, Global Packing Management LARGE UK PHARMA

“We depend on Glemser’s team to provide a combination of business, technical and change management in our Quality department. Their consulting team plays an important role for both new and existing business processes, while understanding the implementation considerations that are so important to our global product portfolio. We depend on Glemser for business process improvements, opportunity resolutions and level two support. Glemser is responsive and dedicated to our success.”

Senior Director of Global Quality, Large NY Pharma

"My company depends on Glemser to provide fast and accurate label support for our global product portfolio. We have been a long-time client and depend upon their staff to support our SPL requirements. Glemser manages all the details and communicates effectively with my team. They are easy to engage and keep us informed of any quality snags throughout the process."

Director, Global Labeling, Large Italian Pharma
INTEGRATIONS

Work within existing systems

ComplianceAuthor® AI provides an authoring experience in a familiar Microsoft Word® format and integrates natively with solutions like Veeva®, SAP®, SharePoint®, Oracle®, and Documentum®, protecting your investment in these products. 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.
Existing systems

See what ComplianceAuthor® AI looks like with your content