DCM-20 Quality Control

More than 50 years ago, the US FDA developed the GLP regulations for careful work and documentation, the extension of which for the production process is GMP. In it, laboratory and manufacturing companies must document how they guarantee error-free work and production, and thus product. Part of this is the care with which production and analysis systems are put into operation and maintained.

The equipment manufacturers themselves must also provide this evidence for their area or make it available to an operator for his own documentation. The tools and documentation of error-free installation and operation are therefore part of quality management.

All this: Sample presentation, reference fluids, IQ/OQ manual and the corresponding OQ protocols are supplied if required or are also carried out by MMAC with a certificate issued.