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.Â
Key Features of the AQ
CAPA Management System
Build Inhouse Participant Database
Run Feasibility Campaigns
Live Recruitment Metrics
In-study Communication Tools
Identification
Evaluation
Investigation
Implementation
Verfication
Effectiveness
Build Inhouse Participant Database
Run Feasibility Campaigns
Live Recruitment Metrics
In-study Communication Tools
Verification
Effectiveness
Identification
Implementation
Evaluation
Investigation
Benefits of Implementing Our CAPA Management System
Enhanced Compliance
Ensure adherence to regulatory standards and guidelines by systematically managing CAPA processes, 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 operations and outcomes.
Audit Readiness Operational Efficiency
Streamline CAPA management 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 priorities and effectiveness, supporting a culture of continuous improvement.
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 the audit management application.
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.
