
by Simplicis
Ensures lab records comply with US FDA 21 CFR Part 11, aiding in error-free audits and data integrity.
Laboratory Information Management System (LIMS)
by Logicon Technosolutions
A scalable platform for Manufacturing Execution Systems and Industrial IoT, integrating with PLC, DCS, cloud, and BI tools for enhanced production efficiency and quality control.
Bioprocess Development & Manufacturingby Syneos
A personalized learning platform that adapts to individual needs, enhancing skill mastery, retention, and real-world impact through AI-driven insights and seamless integration.
Modeling & Simulation
by Greenlight
Provides fast, secure access to patient health records from over 90% of US healthcare providers, streamlining data retrieval for providers, researchers, and insurers.
Clinical Data Integration
by Greenlight
A digital solution for electronic clinical outcome assessments, enhancing study operations with automation and integration capabilities.
Clinical Trial Managementby Certara
AI-enabled biosimulation and strategy to reduce, refine, or replace animal studies in drug development.
Modeling & Simulationby Scilife
Software for managing medical device quality, ensuring compliance with ISO 13485 and FDA 21 CFR 820, and streamlining design controls and documentation.
Regulatory & Quality Complianceby Scilife
Digital solution for managing quality processes, ensuring compliance, and driving continuous improvement in life sciences organizations.
Regulatory & Quality Complianceby Scilife
Software for managing deviations and nonconformities in life sciences, enabling quick event registration and streamlined follow-up actions.
Regulatory & Quality Complianceby Scilife
Software for managing supplier qualifications, audits, and findings in life sciences, integrating with other modules for seamless information access.
Regulatory & Quality Complianceby Scilife
Medical device development software that streamlines traceability, accelerates audit readiness, and ensures compliance with ISO 13485:2016 and FDA 21 CFR 820.
Regulatory & Quality Complianceby Scilife
Track and visualize quality KPIs to improve decision-making and compliance in life sciences.
Regulatory & Quality Complianceby Scilife
Software for managing change requests, approvals, and implementations, fostering company-wide participation in modifications.
Regulatory & Quality Complianceby Scilife
Software for managing equipment qualification, maintenance, and calibration tasks with simple workflows and inspection readiness.
Regulatory & Quality Complianceby Scilife
Centralized document management system for efficient operations, integrating with MS Office and automating essential tasks.
Regulatory & Quality Complianceby Scilife
A user-friendly platform for managing risk assessments, integrating with other processes, and ensuring timely reviews.
Lab Safety & Risk Managementby Scilife
Software to manage Corrective and Preventive Actions (CAPAs) efficiently, ensuring compliance and streamlined workflows.
Regulatory & Quality Complianceby Scilife
Software ensuring FDA 21 CFR 11 compliance by controlling printing and reconciliation, tagging each page for easy identification and retrieval.
Regulatory & Quality Complianceby Scilife
Software for managing employee training in life sciences, ensuring compliance and efficiency with automated notifications and customizable training plans.
Regulatory & Quality Complianceby Scilife
Centralizes design control documentation for medical devices, ensuring compliance with ISO 13485 and 21 CFR part 820 through structured workflows and automated traceability.
Regulatory & Quality Compliance