Search life sciences software.

by Caliber

Instant product quality review reports and analytics for pharmaceutical manufacturers, replacing months of manual work with on-demand compliance and trend analysis.

by Trial Interactive

Issue processing, management, and oversight for clinical trials with incident logging, investigations, CAPAs, and audit tracking.

by TetraScience, Inc.

Data integrity and traceability for GxP-compliant workflows across the product lifecycle.

by Enzyme

Document control, design control, training, risk management, audits, complaints, CAPA, and nonconformance tracking for cGMP and QSR compliance.

by Qualityze

CAPA, audit, compliance, and document control for quality management in regulated industries.

by Circulant Solutions

GLP and GCP-compliant SAS PC validation in secure cloud environment for biopharma analysis.

by Circulant Solutions

GxP-validated SAS cloud access for biostatistics teams with pre-built qualification templates and 21 CFR Part 11 compliance.

by Simploud

Quality event tracking, complaint management, CAPA, change control, and batch record management for life sciences compliance.

by Simploud

Electronic binder for managing design control, verification, validation, and complex project workflows with full audit trails and live traceability.

by Simploud

Centralized document management with version control, approval workflows, electronic signatures, and training tracking for regulated life sciences organizations.

by Simploud

Automated global product registration, variations, and renewals tracking with intelligent timeline calculations and centralized submission management.

by Simploud

Environmental and safety incident reporting, risk mitigation, and regulatory compliance for life sciences and industrial operations.

by Simploud

Supplier onboarding, auditing, and monitoring for regulated industries with centralized document management and compliance tracking.

by Simploud

Risk-based validation with pre-configured templates and traceability for GxP compliance.

by Quality Forward

Quality management and compliance automation for life sciences and regulated industries, including deviations, CAPA, audit management, and document control.

by CIMCON Software

21 CFR Part 11 compliant AI validation, gap assessment, and lifecycle management for pharmaceutical operations.

by CIMCON Software

Automated testing and validation for AI models covering fairness, interpretability, code quality, privacy, and cybersecurity with regulatory compliance.

by CIMCON Software

AI/GenAI/LLM testing and validation with automated risk assessment, inventory management, and 21 CFR Part 11 compliance.

by CIMCON Software

Convert paper forms to 21 CFR Part 11 compliant digital workflows with electronic signatures and data validation.

by CIMCON Software

Document and data management with version control, electronic signatures, and audit trails for 21 CFR Part 11 compliance.