Calibration & Validation

Provide reliable Calibration services of Weighing Balances and weights for accurate measurements. Both on site and lab facility available.

Calibration Ranges

1. 1 . OIML Weights Class F2, E1, E2, M1 & M2, 10 mg to 20 kg
2. 2 . Analytical Balances and Weighing Scales –0 to 60kg

Calibration services for Temperature and Humidity available.

Temperature

1. 1 . Liquid Glass Thermometer, Temperature Gauge, Dial Thermometer etc, Range -80 ºC to 250ºC
2. 2 . RTD, Thermocouple (with or without Indicator), Temperature Indicator, Range -80ºC to 1500ºC
3. 3 . Temperature Indicator of Cold Chambers, Ovens, Incubators, Furnace, Baths etc, Range -80ºC to 1500ºC
4. 4 . Temperature Mapping of Freezer, Ovens, Indicators, Environmental Chambers, Liquid Bath & Data Logger with Sensor, Range -30ºC to 300ºC

Humidity

1. 1 . Humidity Meter, Thermo-Hygrometer etc, Range- 25% to 95%RH @25ºC, 15 to 40 ºC @50%RH.
2. 2 . Condition Chamber, Humidity Indicator etc, Range- 25% to 95%RH @25ºC, 15 to 45 ºC @50%RH.

Calibration services for glassware provided.

Undertake Clean Room Validation test like :

1. 1 . Air Changes Test
2. 2 . Air Borne Particle Count Test
3. 3 . Hepa Filter Integrity Test
4. 4 . Air Flow Pattern Test

Temperature & Rh Mapping for Pharma plants, Hospitals and all critical places where Temperature & Rh play a crucial role.

The Biomedical Calibration is important because they establish whether the medical devices are appropriate, according to the international standards or not. The calibration also helps to minimize misdiagnosis caused by poorly calibrated machine. It is very important to configure hospital systems, according to the standard calibration because these machines need to be absolutely accurate since it is a matter of life and death.

Medical devices can drift away from the measurements due to their internal components. This phenomenon is common among all manufacturers, even with the most advanced ones. Over time, the internal components – both mechanical and electronics wear and tear. As a result, their performance starts to decrease and results in erratic readings. These erratic readings can directly affect the patient life, such as in the case of ultrasound units.

Secondly, as mentioned above, regulatory bodies such as the FDA in the US have made it mandatory for the manufacturers to perform routine calibration and maintain calibration records. Otherwise, the manufacturer is not granted accreditation and is not allowed to start or continue its operations.

The calibration process is necessary to detect these erratic readings and comply with the regional regulatory bodies. The calibration must be regularly performed, and documentation maintained for presenting during a routine inspection.