Features

Features

Features

Artos was designed from the ground up for regulatory and medical writing teams.

Artos was designed from the ground up for regulatory and medical writing teams.

Artos was designed from the ground up for regulatory and medical writing teams.

Content Authoring

Content Authoring

Content Authoring

With powerful AI tools that learn how your company works, the Artos platform turns your experimental and source data into the highest-quality drafts of key documents in regulatory submissions like Clinical Study Reports, Module 2 Summaries, Clinical Evaluation Reports, and more exactly the way your company wants.


Our platform comes complete with tools to help draft much more than just text, too: formatted tabular data, hyperlinks, and more are all easier and faster than ever to manage through the Artos platform.

With powerful AI tools that learn how your company works, the Artos platform turns your experimental and source data into the highest-quality drafts of key documents in regulatory submissions like Clinical Study Reports, Module 2 Summaries, Clinical Evaluation Reports, and more exactly the way your company wants.


Our platform comes complete with tools to help draft much more than just text, too: formatted tabular data, hyperlinks, and more are all easier and faster than ever to manage through the Artos platform.

With powerful AI tools that learn how your company works, the Artos platform turns your experimental and source data into the highest-quality drafts of key documents in regulatory submissions like Clinical Study Reports, Module 2 Summaries, Clinical Evaluation Reports, and more exactly the way your company wants.


Our platform comes complete with tools to help draft much more than just text, too: formatted tabular data, hyperlinks, and more are all easier and faster than ever to manage through the Artos platform.

Workflow Integrations

Workflow Integrations

Workflow Integrations

The process of authoring and managing regulatory submissions is complex and involves lots of systems. Integrate Artos with your document management systems, like Veeva RIM, Box, and more, so that Artos doesn't become another thing you have to manage but a platform that helps you get more work done.


Our integrations allow you to save documents the way your organization is used to, so you can focus on getting the most robust regulatory submissions done in a fraction of the time.

The process of authoring and managing regulatory submissions is complex and involves lots of systems. Integrate Artos with your document management systems, like Veeva RIM, Box, and more, so that Artos doesn't become another thing you have to manage but a platform that helps you get more work done.


Our integrations allow you to save documents the way your organization is used to, so you can focus on getting the most robust regulatory submissions done in a fraction of the time.

The process of authoring and managing regulatory submissions is complex and involves lots of systems. Integrate Artos with your document management systems, like Veeva RIM, Box, and more, so that Artos doesn't become another thing you have to manage but a platform that helps you get more work done.


Our integrations allow you to save documents the way your organization is used to, so you can focus on getting the most robust regulatory submissions done in a fraction of the time.

Powerful Automations

Powerful Automations

Powerful Automations

Automate away all the busywork tasks that make regulatory submissions take forever. Updating data tables in your submission with new data, rewriting summaries of the data; receiving alerts when information you write in one section affects another, hyperlinking your documents, and more can all be easily turned into automations that help put the boring parts of your regulatory submission on auto-pilot.

Automate away all the busywork tasks that make regulatory submissions take forever. Updating data tables in your submission with new data, rewriting summaries of the data; receiving alerts when information you write in one section affects another, hyperlinking your documents, and more can all be easily turned into automations that help put the boring parts of your regulatory submission on auto-pilot.

Automate away all the busywork tasks that make regulatory submissions take forever. Updating data tables in your submission with new data, rewriting summaries of the data; receiving alerts when information you write in one section affects another, hyperlinking your documents, and more can all be easily turned into automations that help put the boring parts of your regulatory submission on auto-pilot.

© 2024 Artos, Inc. All rights reserved.

© 2024 Artos, Inc. All rights reserved.

© 2024 Artos, Inc. All rights reserved.

Interested in learning more?

Contact us at info@artosai.com

Interested in learning more?

Contact us at info@artosai.com

Interested in learning more?

Contact us at info@artosai.com