Quartica MARS Platform

The unified AI platform for medical writing, safety automation, and regulatory compliance.

Safety/Pharmacovigilance Suite

AI automation for PBRER, DSUR, RMP, aRMM, PSMF, PVA, and more.

Clinical Medical Writing Suite

AI medical writing for Protocols, ICFs, CSRs, SAPs, Subject Narratives, Patient Profiles, and more.

Regulatory Affairs Suite

AI automation for CTD, CMC, Ad/Promo documentation, and more.

Manufacturing/Quality Suite

AI automation for APQR, Batch Records, Validation Protocols, CoA, and more.

About Us

Learn about Quartica’s mission, leadership, and AI innovation in life sciences.

Quartica
Customer Experience

Generate regulatory and quality compliant documents Using MARS AI

MARS – Customer Engagement Model

The MARS AI Platform for Life Sciences

Domain Expertise

Feel secure knowing you have a partner with the biopharma domain expertise to ensure the MARS solutions are designed to meet your needs.

Platform Services

Expand your existing deployment into new areas to link upstream and downstream processes with the breadth of MARS platform capabilities.

Validation Services

Our QA team is available to provide you with support assistance and guidance with inspections, audits and other related activities.

Support Services

Our team is available to provide you with support assistance and guidance on supported versions of MARS.

Automation tailored for the specific regulatory & validation
needs of the life sciences industry

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