PLC in Pharmaceutical Industry: High-Quality PLC Programming by Proven Experts

The pharmaceutical industry is one of the industries that is subject to the strictest regulatory requirements and standards. For this reason, quality assurance is seen as one of the most important criteria in the production processes of pharmaceutical companies. Anyone who uses programmable logic controllers in the production of drugs is obliged to ensure that they use particularly high-quality PLC programming. This should comply with all fixed rules, quality standards and norms, almost unconditionally.

Programmable logic controllers (PLCs) in the pharmaceutical industry must meet many requirements, for example the GAMP®5 requirements that have been active since February 2008. GAMP stands for Good Automated Manufacturing Practice. Furthermore, various legal provisions, EU requirements, the PIC / S Guidance, standards of the industry and professional associations and national and international guidelines and quality standards must be complied with. The respective national regulatory authority checks the quality of the computer-aided systems and validates the corresponding PLC programming.

A high-quality PLC programming in the pharmaceutical industry therefore means error-free functionality and correct installation within a defined storage location. Every modification and further development can be traced by validation. The maintenance of the corresponding programs is also possible at any time - thanks to well-structured design and detailed documentation.