Transform Findings into Action
with Zentixs Eye

Efficiently manage internal and external audits, ensuring compliance with GxP and regulatory standards. Enhance transparency, reduce risk, and simplify the audit process to maintain high-quality standards across all operations.

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Auditing Versatility:
One Software, Infinite Capabilities

Audit Planning and Scheduling

  • Tools for scheduling audits based on timelines, resources, and priority.
  • Calendar integration for tracking audit schedules and deadlines.

Audit Checklists

  • Customizable checklists to ensure all relevant criteria are assessed during audits.
  • Pre-defined templates based on industry standards or regulatory requirements.

Document Management

  • Centralized storage for audit-related documents, including policies, procedures, and past audit reports.
  • Version control to manage document revisions and updates.

Non-Conformance Tracking

  • Mechanisms to record and track non-conformances identified during audits.
  • Ability to assign corrective actions and monitor their status.

Reporting and Analytics

  • Tools for generating comprehensive audit reports, including findings, recommendations, and follow-up actions.
  • Analytics to identify trends in audit findings and areas for improvement.

CAPA Management

  • Integration with Corrective and Preventive Action (CAPA) processes to address issues identified during audits.
  • Workflow for documenting and tracking CAPA effectiveness.

Why choose Zentixs Eye

Audit Trail and Compliance Tracking

  • Maintain an audit trail of all actions taken within the software for compliance purposes.
  • Tracking capabilities to ensure adherence to regulatory standards and internal policies.

User Management and Permissions

  • Role-based access controls to restrict sensitive audit information to authorized users.
  • Features for assigning auditors and managing their permissions within the system.
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Integration Capabilities

  • Ability to integrate with other systems, such as Document Management Systems (DMS), Learning Management Systems (LMS), and enterprise resource planning (ERP) systems.

Mobile Access

  • Mobile-friendly interface to allow auditors to access checklists, documents, and record findings on-site.

Training and Resources

  • Access to training materials, guidelines, and resources for auditors to ensure consistent practices.

Industries We Serve

Fragmented processes and siloed teams are now a thing of the past. Seamlessly integrate with diverse industry workflows and regulatory frameworks to streamline critical business functions and save time.

Pharmaceutical Companies

Biopharmaceutical Organizations

Clinical Research Organizations

Clinical Trial Organizations

Analytical Laboratories

Bioanalytical Laboratories

Medical Device Companies

Life Sciences Organizations

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Third-Party Audit
Management Features

  • Tracking of Findings: Effectively track third-party audit findings for documentation and monitoring.
  • CAPA Management: Manage Corrective and Preventive Actions (CAPA) linked to findings.
  • Assignment to Stakeholders: Assign findings to relevant stakeholders for accountability.
  • User Notifications: Automatic notifications to users when findings are assigned.
  • Resolution Guidance: Provides recommended resolutions for addressing findings.
  • Closure of Findings: Allows formal closure of findings after corrective actions are implemented.

Seamless Product Integrations

Connect Eye with the entire Zentixs ecosystem

Zentixs Docs
Zentixs Log
Zentixs Eye
Zentixs Labs
Zentixs Saga
Zentixs Talent
Zentixs Caliber

Seamless Product Integrations

Connect Eye with the entire Zentixs ecosystem

Zentixs Docs
Zentixs Log
Zentixs Eye
Zentixs Labs
Zentixs Saga
Zentixs Talent
Zentixs Caliber

Compliance & Security

Maintain oversight with intelligent monitoring, periodic reviews, and qualification-based access.

21 CFR Part 11

Support compliant electronic records with secure audit trails and electronic signatures.

EU Annex 11

Enable validated computerized systems with strong data integrity controls.

GxP Guidelines

Help organizations align quality processes with global regulatory requirements.

GMP Support

Digitize manufacturing workflows with controlled documentation and process visibility.

GLP Standard

Support laboratory compliance with traceable records and reliable data management.

GCP Protocol

Facilitate compliant clinical documentation and study process management.

ALCOA+ Principles

Promote data integrity with accurate complete and traceable digital records.

ICH Q10 Framework

Support operational quality systems with risk based and standardized processes.

Frequently Asked Questions

Zentixs Eye software is designed to track third-party findings, manage Corrective and Preventive Actions (CAPA), and facilitate the closure of findings in compliance with regulatory standards
Zentixs Eye streamlines the process of tracking audit findings, assigning responsibilities, and ensuring that corrective actions are implemented effectively.
Zentixs Eye allows users to record, monitor, and manage third-party audit findings in a centralized system, ensuring thorough documentation and follow-up.
Yes, you can categorize findings based on severity or type to prioritize corrective actions and streamline management efforts.
Zentixs Eye includes built-in functionalities to manage CAPA, linking findings directly to corrective actions to address issues effectively.
Yes, the software provides tools to track the status of CAPA implementations, ensuring transparency and accountability.
You can easily assign findings to relevant stakeholders within the software, ensuring clear accountability for each finding.
The software automatically sends notifications to users when findings are assigned, prompting timely action and follow-up.
Yes, Zentixs Eye offers recommended resolutions for addressing findings, helping users implement corrective actions effectively.
Yes, users can customize resolution recommendations based on specific organizational practices and regulatory requirements.
Once corrective actions are implemented, users can formally close findings within the software, documenting the resolution process for future reference.
Yes, there is a review process in place to ensure that all necessary steps have been taken before formally closing a finding.