MARS Platform Capabilities

The foundation for medical content generation

Platform Capabilities

The MARS AI Platform for Life Sciences provides enterprise level services by combing cutting edge technology with deep domain knowledge while ensuring compliance with the regulatory standards

Artificial Intelligence

Get up and running within weeks with no lag time to start delivering results with automation models. Empower business users with ability to deliver at a speed, scope and quality that could only be achieved with the aid of intelligent machine computing. With the ability to leverage existing automation models to increase efficiency and productivity organizations can see tangible ROI from projects in the first year.

Workflow Automation

The cloud platform allows life sciences organizations to focus on automating the business processes while leveraging the benefits of pre-configured hardware, infrastructure, and computing costs. The platform provides enterprise-level automation capabilities at a low total cost of ownership, increased security, and accelerated implementations and upgrades

Document Orchestration

MARS platform is configuration driven to meet unique needs tailored for big or small, well defined or development needs using a modular phased deployment delivery approach. The platform also allows organizations to leverage pre-configured business process workflows and regulatory intelligence as a way to simplify processes and reduce implementations cycle times.

Security and Governance

MARS Information Security architecture utilizes an framework to address security governance, protecting information assets and systems against attacks and incidents while ensuring appropriate security is a priority at all levels of the product development process. The MARS platform supports SSO by integrating with customer IDP for authentication and authorization. The MARS Platform adheres to the highest standards, including provisions for data protection, security, privacy, compliance, trust, reliability, and sustainability.

21 CFR Part 11 Compliance

MARS has been designed and developed for compliance with 21 CFR Part 11 regulations.  We test this compliance by design reviews and by tracing specific Part 11 requirements through to functional specifications and Test Suite test cases. We can demonstrate this by providing visibility into the Part 11 requirements, functionality specifications, design, test cases and traceability. Quartica follows documented life cycle processes for computer system validation and training which are part of our QMS.

Discover your clear path to automation excellence using MARS

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