CaliberLIMS® complies with the regulations laid down by the all-important US FDA 21 CFR.
FDA 21 CFR 211.68: Deals with the Suitability & Inspection of Equipment to be used for recording the data.
FDA 21 CFR 211.160: General requirements (4): Deals with the calibration of instruments, apparatus, gauges, and recording devices.
FDA 21 CFR 820.72: Deals with documentation of procedures for utilization of the technical equipment complying with the national or international standards.
CaliberLIMS® has the built-in systems to cater to all the above requirements laid down by the US FDA.