CAPA Management

The AQ CAPA Management System is designed to facilitate the identification, evaluation, and rectification of non-conformances and deviations, thereby enhancing quality control and regulatory compliance in the CAPA process.

Key Features of the AQ
CAPA Management System

Build Inhouse Participant Database

Run Feasibility Campaigns

Live Recruitment Metrics

In-study Communication Tools

Identification

Our system enables quick and accurate identification of issues that require CAPA, streamlining the initiation of corrective or preventive measures.

Evaluation

Integrated risk assessment tools enable prioritised CAPA efforts by evaluating issues based on impact and severity.

Investigation

Streamline action plan creation with clear corrective and preventive steps, responsibilities, and deadlines for effective issue resolution

Implementation

Track CAPA implementation progress in real-time to ensure timely and effective resolution of underlying issues

Verfication

Automatically compile detailed records of CAPA activities, from issue identification to implementation, ensuring audit readiness

Effectiveness

Utilise advanced analytics for CAPA trend, effectiveness, and compliance monitoring over time. Customisable reports offer insights for continuous improvement

Build Inhouse Participant Database

Run Feasibility Campaigns

Live Recruitment Metrics

In-study Communication Tools

Verification

Our CAPA management software automatically compile detailed records of CAPA activities, from issue identification to implementation, ensuring audit readiness

Effectiveness

Our data capture software utilise advanced analytics for CAPA trend, effectiveness, and compliance monitoring over time. Customisable reports offer insights for continuous improvement

Identification

Our CAPA management software enables quick and accurate identification of issues that require CAPA, streamlining the initiation of corrective or preventive measures.

Implementation

Track CAPA implementation progress in real-time to ensure timely and effective resolution of underlying issues

Evaluation

Integrated risk assessment tools enable prioritised Corrective and Preventive Action (CAPA) efforts by evaluating issues based on impact and severity.

Investigation

Our health care system streamline action plan creation with clear corrective and preventive steps, responsibilities, and deadlines for effective issue resolution

Benefits of Implementing Our CAPA Management System

Enhanced Compliance

Ensure adherence to regulatory standards and guidelines by systematically managing the CAPA process, reducing the risk of non-compliance penalties.

Improved Quality Control

Identify and rectify potential issues before they escalate, maintaining the high quality of clinical trial management and outcomes with clinical research SaaS technology.

Audit Readiness Operational Efficiency

Streamline CAPA management system processes through automation, reducing manual efforts and enabling a more efficient resolution of issues. Linked with the audit management system giving a comprehensive quality control.

Data-Driven Decision Making

Utilise comprehensive data and analytics to make informed decisions regarding CAPA process priorities and effectiveness, supporting a culture of continuous improvement in the health care system.

Audit Readiness

Maintain detailed, organised records of all CAPA activities, ensuring that your trial is always prepared for internal or regulatory audits and management of audits using corrective and preventing action in the CAPA process.

Learn how our CAPA Management System can transform your approach to quality management and compliance. Contact us today to schedule a demonstration and explore the critical role our system can play in enhancing your clinical trial success.

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