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SERVICES

NIVII LABS PVT LTD delivers accredited-grade calibration, validation and maintenance services for regulated industries. Click any service below to jump to detailed scope, deliverables and FAQs.

Precision calibration of pressure, temperature and humidity instruments.
Ensuring reliable temperature mapping and controlled thermal conditions.
Validation of cleanrooms and air handling systems for compliance.
Validation of compressed and nitrogen air systems for safety and quality.
Testing and validating pure steam systems to meet regulatory standards.
Complete chamber maintenance with documentation and compliance support.
Calibrations

Calibrations

NIVII LABS PVT LTD provides traceable calibrations for pressure, temperature, humidity, electrical and dimensional instruments. Calibrations are performed to documented procedures using calibrated master standards with stated measurement uncertainty and traceability to national standards.

Services available in-lab or on-site to reduce downtime. Each job receives a calibration certificate with result tables, environmental conditions, uncertainty statement and technician details.

Traceable, auditable calibration certificates – ready for quality systems and audits.

What we do

  • Pressure, temperature, humidity and electrical calibration
  • In-lab precision services and on-site calibrations
  • Certificate with uncertainty, traceability and recommendations

Applications & markets

  • Pharmaceutical production and QC laboratories
  • Food & beverage process controls
  • Automotive, electronics and general manufacturing

FAQs

Instrument details, measurement results, measurement uncertainty, traceability statement and environmental conditions.
Yes — on-site calibrations are planned to maintain measurement conditions and reduce interruption to production.
Thermal Validations

Thermal Validations

We perform comprehensive thermal mapping and cycle qualification for ovens, autoclaves, stability chambers and temperature-controlled equipment. Mapping uses calibrated data-loggers and precision sensors to characterise temperature distribution and identify hot/cold spots.

Deliverables include mapping reports, statistical analysis, IQ/OQ/PQ documentation and recommendations for corrective actions where required.

Validated thermal processes reduce product risk and ensure reliable batch outcomes.

What we do

  • Multi-point temperature mapping with calibrated loggers
  • Cycle qualification (IQ/OQ/PQ) and data analysis
  • Validation reports and re-mapping after adjustments

Applications & markets

  • Sterilizers and autoclaves
  • Stability chambers and environmental testing
  • Ovens and heat treatment equipment

FAQs

Duration depends on chamber size and protocol; mapping can take hours to days depending on the study requirements.
Yes — full qualification documentation, raw data and executive summaries are provided for audits.
HVAC Validations

HVAC Validations

NIVII LABS PVT LTD validates HVAC systems, air handling units (AHUs), HEPA/FFU installations and cleanroom environments. Services include airflow mapping, differential pressure checks, particulate monitoring and environmental trend analysis.

Reports include test results, gap analysis and remediation recommendations to keep your controlled environments compliant.

Robust HVAC qualifications protect product quality and ensure regulatory readiness.

What we do

  • Airflow, velocity and volumetric measurements
  • Differential pressure, leakage and HEPA integrity tests
  • Particulate and environmental monitoring with trend reports

Applications & markets

  • Pharmaceutical & aseptic processing
  • Medical device cleanrooms
  • Food processing and semiconductor facilities

FAQs

Frequency depends on system criticality; many sites run quarterly or biannual checks with annual requalification.
Yes — we perform HEPA integrity, face velocity and FFU performance testing as part of cleanroom qualification.
Compressed / Nitrogen Air

Compressed / Nitrogen Air Validation

Compressed and nitrogen air systems are validated for purity, dew point, pressure stability and contaminants. These services protect product quality and downstream equipment from moisture and oil carryover.

Our validation includes dew point measurement, oil/particulate sampling, pressure profiling and system audits. We provide remediation recommendations and routine monitoring programs.

Validated instrument air prevents contamination, supports sterility and protects product integrity.

What we do

  • Dew point, moisture and oil carryover testing
  • Pressure, flow and leakage analysis
  • Purity sampling and ongoing monitoring programs

Applications & markets

  • Instrument air for pharma and laboratory use
  • Food & beverage packaging gases
  • General manufacturing and process applications

FAQs

We test dew point, oil and particulate content, pressure stability, and purity where required.
Periodic checks depend on usage and criticality; high-risk processes may require monthly or quarterly checks.
Pure Steam Validations

Pure Steam Validations

Pure steam systems used for sterilization and process applications are tested for steam quality, condensate contamination and correct distribution. We measure conductivity, carryover and perform condensate sampling.

Validation packages include test results, analysis, corrective actions and documentation suitable for audits.

Ensuring steam quality is critical for sterilization integrity and product safety.

What we do

  • Steam quality testing and condensate analysis
  • Distribution checks and system performance audits
  • Validation reports aligned with regulatory expectations

Applications & markets

  • Sterilizers and steam-in-place (SIP) systems
  • Pharmaceutical and medical device sterilization
  • Process steam in food and biotech

FAQs

Steam quality relates to dryness fraction, carryover and condensate contamination; we test conductivity and particulate carryover.
Yes — we provide SIP validation protocols and sampling to verify system performance.
Chambers Maintenance

Chambers Maintenance & Documentation

Preventive maintenance, calibration and documentation for environmental and process chambers (stability, climatic, humidity and thermal chambers). We provide scheduled servicing, repairs, spares recommendations and full compliance packs.

Services include periodic performance checks, re-calibration after repairs, temperature & humidity mapping and handover documentation for quality records.

Proactive maintenance extends equipment life and ensures reliable validation results.

What we do

  • Scheduled preventive maintenance and calibration
  • Repair coordination, spare parts advice and performance checks
  • Complete service records and compliance documentation

Applications & markets

  • Stability chambers and climatic test equipment
  • Pharma R&D and production environments
  • Quality control and environmental testing labs

FAQs

Yes — AMC packages are available for scheduled calibration, maintenance and priority response.
Yes — re-mapping and qualification after repair or major adjustment is recommended and offered.
CALL US NOW
Mobile: +91 63029 80996
Mobile: +91 77995 40799
VISIT OUR OFFICE
Sri Satya Sai Nagar Colony,
4-178/3, RCI Road,
Jillelguda, Hyderabad - 500097
EMAIL US
General: info@niviilabs.com
Service: service@niviilabs.com