Search life sciences software.

by Labguru

GxP-compliant cloud environment with continuous validation for research data integrity and quality assurance.

by Qualcy

Document control, risk management, and regulatory compliance automation for pharmaceutical and medical device companies, with AI-powered regulatory change monitoring.

by QSI Technologies, Inc.

Document management, training, and workflow automation for regulatory compliance and quality initiatives.

by QSI Technologies, Inc.

Design and automate customized forms with multi-step workflows, routing, notifications, task assignment, and electronic signatures for quality compliance processes.

by QSI Technologies, Inc.

Competency testing and skills assessment for regulated companies, with customizable quizzes, rotating questions, and performance tracking to verify employee training and identify knowledge gaps.

by QSI Technologies, Inc.

Centralized change request lifecycle management with document attachment, electronic routing, and multi-stage review and approval workflows.

by QT9 Software

Centralize quality management across 25+ modules with pre-validated compliance for ISO, FDA, and EU MDR standards. Implement in under 30 days.

by Instem

Quality management and compliance automation for regulated organizations, with modules for CAPA, audits, change management, and IT governance.

by Certara

Publish, validate, and review eCTD submissions for regulatory acceptance.

by Valiance Partners

Complex data migration for life sciences applications with configurable rules, no coding required.

by Valiance Partners

Automated data, content and ETL testing for 100% pre- and post-migration verification and compliance validation.

by Valiance Partners

Job management and execution control for organizing and automating complex migration and consolidation projects.

by Valiance Partners

Data archiving and extraction for GxP systems, with configurable migration to any archive target.

by Clarivate Plc

AI-assisted regulatory intelligence for navigating global pharma compliance and strategic decision-making.

by Clarivate Plc

Global chemistry, manufacturing, and controls (CMC) regulatory intelligence for drug development and market access.

by TrialAssure

Clinical trial registration and results disclosure across 40+ global registries from a single portal.

by TrialAssure

Track global compliance across clinical trial registration, results disclosure, data sharing, and transparency activities in real time.

by Cytodyme

Post-market complaint management, regulatory reporting, and literature surveillance for medical device companies.

by Cytodyme

Monitor real-world safety signals, screen published evidence, and generate regulatory post-market reports with AI-assisted analysis.

by Cytodyme

Capture, classify, and review complaints across multiple sources with AI-assisted coding and real-time risk monitoring for regulatory compliance.