Drug Discovery Trials Workflow Housing Platform

    Move fast. Scale up. Stay agile and audit ready.

    GxP Track℠ gives drug discovery teams the tools to speed up R&D while maintaining full traceability and regulatory organizational data compliance. Log every experiment, assign protocols, and respond to deviations. All without slowing innovation.

    FDA 21 CFR Part 11

    Compliance Friendly

    EU Annex 11

    Compliance Friendly

    ISO 27001

    Compliance Friendly

    SOC 2

    Compliance Friendly

    Flexible tools for regulated R&D

    From lab-based research to preclinical handoffs, GxP Track℠ keeps your operations traceable, scalable, and inspection-ready.

    Adapt quickly

    Use configurable workflows that evolve with your research. Support changing teams, protocols, & study designs without rework.

    Track everything

    Automatically log each step under a verified user ID. Maintain audit-ready records with full traceability - no manual effort.

    Align with protocol

    Link SOPs directly to tasks & experiments. Keep teams on the same page & reduce deviations across studies.

    Spot issues early

    Surface risks faster & make smarter decisions, sooner.

    Seeking Phase I Participant Organizations (Confidential Source Code Disclosure Considered)

    Others slow you down.

    GxP Track℠ speeds you up.

    Other solutions

    No audit-ready research logs
    Rigid tools that don't fit R&D
    Delayed deviation reporting
    Unstructured or siloed documentation

    GxP Track℠

    Real-time, user-tagged activity tracking
    Flexible SOPs & workflows for discovery
    Instant logging & linked CAPA workflows
    Automated, validated, traceable records

    Built for discovery. Ready for inspection.

    Maintain regulatory organizational data compliance from day one. GxP Track℠ helps you log, track, and scale discovery work without slowing down innovation.

    Dynamic protocol management

    Create, edit, and deploy evolving SOPs as research progresses - with built-in version control, change history, and role-based approvals. Ensure everyone is working from the latest, auditable process without slowing innovation.

    Role-based training & assignments

    Automatically assign training and documentation updates based on team roles or departments. Track completions and escalate overdue tasks to maintain alignment and organizational data compliance across rapidly shifting study conditions.

    Experiment logging

    Capture every step of an experiment - from setup to outcome - with full context, including user identity, timestamp, and linked protocols. Build a traceable record that supports both reproducibility and regulatory inspection.

    Deviation reporting & follow-ups

    Flag anomalies or deviations as they happen, directly within the logged event stream. Trigger linked investigations, CAPAs, or protocol updates - keeping quality control responsive and fully documented.

    Structured data streams

    Export experiment logs in clean, queryable formats (JSON, CSV, etc.) to your analytics tools or dashboards. Spot trends, generate insights, and prep for audits without formatting headaches or missing data.

    Speed + precision = success

    Check periodically for case study updates.

    80%

    Striving for faster review & release

    100%

    Striving for right-first-time output

    50%

    Striving for reduction in processes

    Connected tools for every sector

    Explore GxP Track℠ modules tailored for regulated research and production workflows, whether you're running early-stage trials or scaling commercial output.

    Life Sciences

    Clinical Trials

    Medical Device

    Drug Discovery

    Pharmaceutical Companies

    From research protocol traceability to FDA-ready batch release, GxP Track grows with your operation. Faster innovation. Stronger organizational data compliance. Smoother cross-functional handoffs.

    Built for breakthroughs. Ready for audits.

    See how GxP Track℠ simplifies organizational data compliance, speeds up documentation, and gives your team more time to focus on research.