Pharmaceutical Calibration Services in Bangladesh
GMP-aligned calibration, equipment qualification and thermal mapping — accredited to ISO/IEC 17025:2017, documented the way DGDA and WHO-GMP audits expect.
What We Calibrate for Pharmaceutical Manufacturers
Autoclaves & Sterilisers
Temperature and pressure validation for autoclaves and dry-heat sterilisers, with as-found/as-left data.
Cold Rooms & Warehouses
Thermal mapping of cold rooms, walk-in chillers and warehouse zones per your qualification protocol.
Cleanroom & Compressed Air
Particle count, airflow, differential pressure and compressed air quality testing for classified areas.
Weighing & Balances
Analytical and platform balance calibration traceable to certified reference weights.
Process Instrumentation
Pressure, temperature, humidity and pH instrument calibration across production and QC.
Equipment Qualification
DQ/IQ/OQ/PQ documentation for new and existing critical equipment.
Why This Matters for a DGDA or WHO-GMP Audit
- Traceable references — every standard we use traces to a national or international metrology institute
- Stated measurement uncertainty — on every certificate, per parameter
- As-found / as-left data — the drift record an auditor asks to see
- QR-verifiable certificates — checked online, by anyone, in seconds
Documentation Ready for Your Quality File
- Calibration certificate with BAB-accredited scope
- Thermal mapping report with data logger plots
- DQ/IQ/OQ/PQ protocol and summary report
- Instrument master list with next-due dates
Related Services
Pharmaceutical Validation
DQ/IQ/OQ/PQ equipment qualification in detail.
Compressed Air & Cleanroom
Cleanroom classification and compressed air quality testing.
Pharmaceutical Calibration FAQs
Are your certificates accepted in DGDA inspections?
Our certificates are issued under BAB accreditation to ISO/IEC 17025:2017 with stated measurement uncertainty and traceable references — the standard DGDA and WHO-GMP inspections expect to see.
Can you calibrate on-site inside a classified cleanroom?
Yes, our engineers follow your gowning and entry procedures and carry out calibration and mapping inside classified areas without compromising your environment.
Do you provide DQ/IQ/OQ/PQ for new equipment?
Yes — see our dedicated pharmaceutical validation service for equipment qualification protocols and reports.
How often should pharmaceutical instruments be calibrated?
Typically annually for most process instruments, with more frequent intervals for critical or high-drift equipment as defined in your calibration master plan.