PLC validation is a requirement which is performed in pharmaceuticals, medical equipment manufacturing, genetics research, and biotechnology. It requires broad documentation, including systems, test information, synopsis reports, and confirmation structures. This documentation gives clients a serious level of certainty that a PLC will reliably give control data or information that meets foreordained determinations. Approval is particularly gainful for machines that utilization the product, which is continually changing to meet the intricate requirements of its clients. The capacity to show that a PLC is acting as expected is likewise a sound business practice.
DAC INFO has a decade of experience in performing PLC validation activity. Our team is specialized in the stringent requirement emphasis GAMP 5 Guidelines, EU Annex 11, and 21 CFR part 11 requirements.
Our team has a successful track record for complex project completion within stipulated timelines for PLC validation in line with requirements for GAMP 5, EU Annex11, and 21 CFR part 11.
Our services offering include BMS Validation, DCS Validation, and customized SCADA validation.