We offer services for the development of qualification documentation (DQ – Design Qualification, IQ – Installation Qualification, OQ – Operational Qualification, PQ – Performance Qualification), in accordance with the requirements of the GMP and current legal guidelines. We focus on process reliability, system and equipment consistency, as well as long-term stability and production quality.
The basis of our company’s approach is the identification of risk at all stages of the design, execution and qualification of industrial and pharmaceutical facilities. We focus on critical points of the process and systems, optimize resources and propose control measures where the risk is highest, thereby ensuring the safe, efficient operation of facilities in accordance with the law.
