Our equipment is designed according to good manufacturing practices for pharmaceutical and biotechnology-sector applications.

The Good Manufacturing Practice GMPefer to medicinal products for human use, and define the requirements that must be met during the development, production and testing phases. In order for a medicine to be deemed safe and effective, the GMP-dictated guidelines must be observed. A fundamental requirement that guarantees pharmaceutical quality. Only by strictly adhering to the GMPs during all the production process phases and the inevitable analysis that follows, can the subsequently produced medicines be deemed effective and safe. More specifically, GMP washing equipment therefore prevents potential contamination during the various processes and keeps the different batches or products disinfected. They ensure that the washing effectiveness meets high quality standards. The processes are easy to repeat, check and validate.

We also design good manufacturing practice-compliant equipment for research or microbiology laboratory applications.

The Good Laboratory Practices (GLP)define the organisational procedures and principals by which laboratory research for non-clinical trials is planned, conducted, controlled, recorded and reported. he GLP principles have been designed to promote the quality and validity of experimental data generated and used to determine the safety of substances contained in pharmaceuticals, pesticides, cosmetic products, veterinary medicines, food additives, feed additives and industrial chemicals, unauthorised for humans. The quality level of such data must be compared with those of other countries in order to make them mutually acceptable in all countries involved. Before GLP compliance certifications are issued, it is usually subjected to periodic checks and inspections. More specifically, the GLP washing equipment is sized to ensure that the various components used in R&D laboratories can be disinfected. They ensure that the washing effectiveness meets high quality standards. The processes are easy to repeat, check and validate.