Artos

Artos is an AI-powered document creation and management platform for life sciences teams, covering the document lifecycle across the CTD pyramid from raw data to final draft. It supports regulatory document types including INDs, NDAs, and BLAs, with content spanning non-clinical and clinical overviews and summaries, tabulated summaries, quality overall summaries, justifications of specifications, analytical validations, clinical study reports, and investigator's brochures.

Core capabilities include Document Drafting, Custom Templates, Section Regeneration, Downstream Visualization, Source Traceability, Audit Logs, Search, and Automations. Integrations connect with document management systems such as Veeva, SharePoint, Google Drive, and Box. Security features include no AI training on customer data, data isolation, zero data retention, access control, audit logs, and SOC II and GDPR compliance. Workflows are tailored to teams including Medical Writing, CMC, Regulatory Affairs, Regulatory Intelligence, IT, and Engineering.

Artos is built for organizations of varying sizes, from small to large pharma and biotech, as well as CROs and medical writing firms. Pricing is seat-based with monthly and yearly billing: a Basic plan for individuals or small teams with 1–2 seats, and an Enterprise plan for 3+ seats that adds integrations, custom templates, private deployments, custom AI, and deployment support.