AQ's Quality Management System for Clinical Research
- Our state-of-the-art Quality Management System (QMS), meticulously crafted to elevate the standards of quality assurance in the realm of clinical research. Our QMS offers a comprehensive suite of tools and features designed to streamline quality management processes and enhance the efficiency and integrity of clinical trials.
Key Features Of AQ's QMS
DMS
CAPA
Management
Training and
compliance
Audit management
Key Features Of AQ's QMS
Audit
Management
DMS
CAPA
Management
Training and compliance
Why Choose AQ's QMS?
Efficiency and Productivity
Streamlined processes and automated workflows to reduce manual effort and administrative overhead.
Time-saving features such as document templates, automated notifications, and task reminders.
Compliance and Regulatory Assurance
Comprehensive compliance features to ensure adherence to regulatory standards such as FDA, EMA, and ICH guidelines.
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Built-in validation and audit trails to support regulatory inspections and audits
Visibility and Insights
Advanced reporting and analytics capabilities to provide stakeholders with real-time visibility into quality metrics, performance trends, and compliance status.
Customisable dashboards and KPI tracking for actionable insights and informed decision-making.
Seamless Integration
Streamline your clinical trials with the AQ platform
A unified solution for a 360-degree view for research. Our integrated quality and operational tools boost efficiency, backed by strict quality control. Elevate research with our robust Quality Management System (QMS) and operational excellence, crafted for precision and progress.
- Comprehensive compliance features to ensure adherence to regulatory standards such as FDA, EMA, and ICH guidelines.
- Built-in validation and audit trails to support regulatory inspections and audits.
