Equipment & Utility Qualification

In regulated pharmaceutical environments, equipment and utilities directly impact product quality, data integrity, and patient safety. Proper qualification and validation are not optional - they are essential components of GMP compliance

At InPharma Solutions, we provide comprehensive qualification and validation services for critical equipment, utilities, and controlled environments. Our approach is systematic, risk-based, and aligned with global regulatory expectations. We ensure your systems perform reliably - today and during inspection

Installation & Calibration Coordination

Proper installation and calibration form the foundation of equipment reliability and compliance. We ensure that every instrument and equipment piece is installed correctly, calibrated accurately, and documented thoroughly because qualification begins with control

We provide:

• Installation Qualification (IQ) protocol development & execution
• Operational Qualification (OQ) planning & testing
• Performance Qualification (PQ) coordination
• Calibration master plan preparation
• Vendor coordination & documentation review
• Traceability to national/international standards
• Calibration interval justification
• Asset identification & tagging strategy

Fume Hood Testing

Fume hoods are critical engineering controls that protect personnel and maintain laboratory safety. Our testing ensures effective containment, personnel safety, and compliance with GMP and laboratory safety standards

We provide comprehensive testing services including:

• Face velocity measurement
• Airflow visualization (smoke pattern test)
• Containment verification
• Sash position verification
• Alarm functionality check
• Periodic performance requalification

LAF (Laminar Air Flow) Qualification

Laminar Air Flow units are essential for aseptic operations and contamination control. We ensure your LAF systems maintain unidirectional airflow and controlled environments as per regulatory expectations

Our qualification services include:

• Air velocity measurement
• HEPA filter integrity testing
• Particle count verification
• Airflow pattern (smoke) studies
• Recovery time studies
• Differential pressure monitoring

Cleanroom Qualification

Our validation ensures your cleanroom classification meets ISO and GMP standards. We provide complete cleanroom qualification services:

• Airborne particle count testing
• HEPA filter integrity testing
• Airflow visualization studies
• Air change rate verification
• Differential pressure mapping
• Recovery studies
• Environmental monitoring program support

HVAC Validation

Our validation ensures stable environmental control and regulatory compliance. HVAC systems are the backbone of environmental control in pharmaceutical facilities

We provide:

• Airflow balancing studies
• Temperature & humidity performance verification
• Air change rate calculation
• Pressure cascade verification
• Filter integrity testing coordination
• System requalification support
• Seasonal performance review

Temperature & Humidity Mapping

Controlled storage conditions are critical for product stability and regulatory compliance. We ensure your storage environments maintain uniform and compliant conditions throughout the area

We provide mapping services for:

• Warehouses
• Cold rooms
• Stability chambers
• Incubators
• Ovens
• Controlled storage areas

Our services include:

• Protocol preparation
• Data logger placement strategy
• Worst-case location identification
• Statistical data analysis
• Excursion analysis
• Final report preparation