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Calibration & Qualification Services | Silicon PharmaEdge

Calibration & Qualification Services

At Silicon PharmaEdge Solutions, we deliver accurate, traceable, and compliant calibration and qualification services that ensure your equipment, systems, and facilities perform exactly as intended. Our services align with GMP, ISO, WHO, EU GMP and global regulatory expectations — supporting pharmaceutical, biotechnology, healthcare, and regulated industries. We don’t just test equipment — we ensure compliance, reduce operational risk, and safeguard product quality.

Calibration Services

Accurate measurement is the foundation of quality, safety, and regulatory compliance. Our calibration services ensure reliable, repeatable, and traceable results while minimizing deviations and audit observations.

Volume Calibration

Precise calibration of volumetric equipment for accurate liquid measurement and dispensing.

  • Pipettes and dispensers
  • Measuring cylinders and volumetric vessels
  • Liquid transfer and dosing systems

Mass (Weight) Calibration

Verification of balances and weighing systems using traceable standard weights.

  • Analytical and precision balances
  • Floor and platform scales
  • Production weighing systems

Temperature Calibration

Ensuring temperature accuracy for product stability and process control.

  • Thermometers and probes
  • Incubators, ovens, chambers
  • Refrigerators and freezers

Pressure Calibration

Calibration of pressure instruments in critical utilities and manufacturing systems.

  • Pressure gauges and transmitters
  • Autoclaves and compressed air systems
  • HVAC pressure monitoring devices

Our Expertise in Action

Calibration Lab Validation Process

Qualification & Validation Services

We confirm that equipment, systems, and processes are fit for their intended use, operate within defined parameters, and meet regulatory requirements.

Equipment Qualification (IQ, OQ, PQ)

  • Installation Qualification (IQ)
  • Operational Qualification (OQ)
  • Performance Qualification (PQ)
  • Inspection-ready documentation
  • Reduced operational risk
  • Improved process reliability

Thermal Mapping

  • Warehouses and storage areas
  • Cold rooms and refrigerators
  • Incubators and stability chambers

Autoclave Validation

  • Temperature distribution testing
  • Pressure & exposure verification
  • Proven sterilization effectiveness
  • Reduced contamination risk
  • Regulatory-compliant validation reports

HVAC Validation

  • Air change rates
  • HEPA filter integrity
  • Temperature & humidity control
  • Differential pressure

Process & Utility Validation

  • Purified Water (PW) and WFI systems
  • Compressed air and process gases
  • Manufacturing and cleaning processes

Why Choose Silicon PharmaEdge Solutions?

  • ✔ Regulatory and GMP-focused approach
  • ✔ Experienced calibration and validation professionals
  • ✔ Traceable and auditable documentation
  • ✔ Risk-based, practical solutions
  • ✔ Support for audits and inspections

Silicon PharmaEdge Solutions — Your partner in compliance, quality, and reliability.

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