Test Equipment Calibration Requirements

A1 4 furnace weigh scales shall be verified quarterly quarterly and calibrated annually at a minimum.

Test equipment calibration requirements. The principle guiding document for requirements relating to in house calibration activities is iso iec 17025 general requirements for the competence of calibration and testing laboratories. Some may require certified and calibrated test equipment regardless of the project size and some may not require stringent calibration standards. A1 9 requires hardness testing equipment be calibrated at least annually. Reference documents 3 1 xxx quality manual 3 2 procedure for quality control 4.

A1 5 requires minimum annual calibration of dewpointers 3 gas analyzers spectrometers ad combustion analyzers. Process and test equipment requirements. Purpose this procedure specifies the schedule and requirements for calibration performance verification and maintenance of laboratory testing instruments and equipment. Calibration standards used for inspection measuring and test equipment shall be traceable to national or international standards.

These requirements may not be explicitly stated which is why you must review the specs before the test. This is verified by an independent accrediting body operating under iso17011. Standard that sets compliance guidelines for calibration laboratories and measuring and test equipment. Then perhaps adjusting the calibration tolerance for the gauge would be a better solution.

This time dependent behavior can be compared to the accuracy requirements of the particular application to determine an initial recalibration interval. Every project and measurement job has a different calibration requirement. If the calibration is performed at 100 units the 1 standard would actually be anywhere between 99 and 101 units. Scope this procedure applies to the laboratory equipment used by the laboratory of xxx.

The manufacture of medical devices makes use of various types of equipment and measuring instruments ranging from simple temperature sensors weighing balances pressure gauges micrometers for measuring dimensions to more complex ones. Manufacturing medical devices is a highly complex process and calibration requirements according to iso 13485 mean high precision and close monitoring. Prescribes general requirements for the competence of calibration and testing laboratories. Subsequently recalibration reports should include as submitted and post calibration accuracy and precision data to validate and or refine the interval.