Turn complaints into organizational data compliance wins

    GxP Track℠ makes it easy to journal adverse effects, assign follow-ups, and stay inspection-ready - without manual logs or siloed records. Capture, triage, and resolve quality issues with full traceability.

    Trusted by industry experts

    Incomplete logs mean red flags are invisible

    Without proper systems, critical complaint data goes unlogged or unresolved. This increases the risk of repeat issues, regulatory scrutiny, and damage to your reputation.

    Complaints logged across emails or spreadsheets

    No connection between issues, follow-ups, & protocols

    Adverse effects missed or poorly documented

    Delayed resolutions and inconsistent responses

    Manual complaint handling isn't just a headache. It can be dangerous in regulated fields. You need traceable, centralized oversight.

    Get in front of every quality concern

    GxP Track℠ turns every issue into a traceable action - helping you close the loop quickly and prove it when it counts. Solve complaints faster. Stay audit-ready.

    Solve issues

    Log complaints & adverse effects from any source & connect them to the relevant product, lot, or process.

    Clear ownership

    Assign tasks and track resolutions across departments with automatic logging. Maintain accountability always.

    Linked workflows

    Tie complaints to CAPAs, SOPs, or audit events to give issues the right context & accountability.

    Audit-ready records

    Maintain complete, timestamped logs for every issue - searchable & exportable in seconds.

    Make complaints handling a breeze

    Log complaints, assign actions, and maintain full traceability from a single powerful system.

    Complaint intake forms

    Document all issues clearly from the get-go. Capture structured complaint data using configurable fields, automated triggers, and severity levels.

    Adverse event journaling

    Make follow-ups faster and easier to audit. Log medical or operational adverse events with full context, including supporting files, categorization, and timestamps.

    Response assignment

    Automatically route issues to the right users or departments, ensuring nothing slips through the cracks and every action is accountable and time-stamped.

    Linked investigations

    Give teams the full picture and reduce the risk of isolated or incomplete resolutions by tying each complaint to CAPAs, deviations, SOPs, or audits.

    Exportable logs

    Instantly generate clean, traceable reports for inspections or internal reviews - with every action, user, and update clearly documented.

    Protect quality, reputation & organizational data compliance

    GxP Track℠ gives high-stakes industries the tools to take action fast.

    Pharmaceutical

    Log patient-reported effects & link to batches, CAPAs, or recalls.

    Document lab-related issues & assign resolution across cross-functional teams.

    Consulting

    Help clients implement audit-ready complaint handling systems.

    Centralize client complaint data & streamline resolution workflows.

    Medical Device

    Record device-related complaints & track issue frequency or severity.

    Technology

    Track product issues and user feedback with full traceability.

    CDMO

    Manage complaints across multiple client products and processes.

    Check out the full quality kit

    Explore the modules working together to give you full lifecycle visibility. Pick what you need. Skip what you don't.

    Audit management
    Protocol management
    Protocol-guided training
    Supplier auditing & management
    Internal audits & self assessments
    Quality systems with customizability

    Build stronger processes with connected tools for investigation, resolution, and reporting.

    Streamline issue resolution

    Book a demo to see how GxP Track℠ makes adverse event logging and complaint resolution seamless, searchable, and audit-ready.