Overview
Transforming CQV - Commissioning, Qualification & Validation
Ensure regulatory compliance and system reliability through comprehensive commissioning, qualification, and validation services. Our expert team delivers validated systems that meet cGMP requirements and industry standards.
Key Benefits
Ensure regulatory compliance and audit readiness
Reduce validation lifecycle costs
Accelerate system deployment timelines
Minimize compliance risks and deviations
Core Capabilities
Commissioning & Qualification (IQ/OQ/PQ)
Computer Systems Validation (CSV)
Process Validation & Revalidation
Equipment Qualification
Cleaning Validation
Solutions in Action
How We Help
Real-world applications of our cqv - commissioning, qualification & validation expertise
IQ/OQ/PQ Execution
Comprehensive qualification protocols for equipment, facilities, and systems ensuring cGMP compliance.
Computer System Validation
End-to-end CSV services from requirements gathering through validation and ongoing compliance.
Process Validation
Statistical process validation studies demonstrating consistent product quality within specifications.
Equipment Qualification
Installation, operational, and performance qualification for manufacturing equipment.
Cleaning Validation
Validation of cleaning procedures to prevent cross-contamination between product batches.
Method Validation
Analytical method validation and transfer supporting regulatory submissions and manufacturing.
eVAL Systems Implementation
Implementation and optimization of electronic validation systems for automated validation lifecycle management and compliance tracking.
Risk-Based Validation by Design
Strategic validation approach using risk assessment methodologies to optimize validation scope and resources based on patient safety impact.
AI-Based Risk Prediction & Automated Validation Tasks
AI-powered risk prediction models and intelligent automation of validation tasks to enhance efficiency and reduce validation cycle times.
