Artos is an AI-based document drafting platform designed for life sciences teams to automate the creation of regulatory submission packages, including INDs, NDAs, and BLAs. By integrating data management, drafting, and quality control, Artos enhances efficiency and accuracy in the document lifecycle, addressing the complexities of compliance in the industry.
Funding
$500K raised to dateRaised to date based on public sources. This may differ from the amount the company actually raised and is based only on what is publicly available on the internet.
Founders
Product
Problem
Life sciences organizations face significant challenges in creating and managing regulatory submission documents, such as INDs, NDAs, and BLAs, due to the complexity of compliance requirements and the need for accuracy across the document lifecycle. Traditional document drafting processes often rely on standalone tools, leading to inefficiencies in data management, version control, and quality assurance.
Solution
Artos is an AI-powered platform designed to streamline document creation and management for life sciences teams, offering an end-to-end suite of features that handles source data, drafting, and quality control. The platform leverages AI purpose-built for each document by cross-functional subject matter experts and AI researchers. Artos integrates data management, drafting, and quality control, enhancing efficiency and accuracy in the document lifecycle. It provides tools to kickstart and streamline processes for medical writing, automate and visualize key processes for CMC, and efficiently pull everything together for regulatory affairs.
Target Audience
Artos is designed for medical writing, CMC, regulatory affairs, regulatory intelligence, clinical operations, IT, and engineering teams within big pharmaceutical, small to mid-sized pharmaceutical, biotech, large med device, small med device, and CRO organizations.
Features
- AI-powered document drafting for Non-Clinical Overviews, Clinical Overviews, and Pharmaceutical Written Summaries
- Downstream visualization to track data and content across all documents
- Source traceability to sync data effortlessly across devices and platforms
- Custom templates and section regeneration for efficient document creation
- Audit logs and search functionality for enhanced data management
- Automations to streamline key processes
- Tools for medical writing, CMC, regulatory affairs, regulatory intelligence, clinical operations, IT, and engineering teams