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.

Careers

Careers

Quartica offers a high-growth, entrepreneurial environment that blends diverse disciplines in life sciences, informatics, information technology, and software engineering. We offer attractive compensation including stock options, benefits, and most importantly, a friendly and exciting work environment. Interested candidates, please send a resume along with salary requirements to the attention of Human Resources

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

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