pharmaceutical industry
Pharmaceutical mechanical engineering
Whether small devices or complete systems - from prototype construction to series production, you can rely on us
Our specialists manufacture with the highest quality standards.
In addition, we also offer engineering and automation services if required. We conceptualize, design, develop, construct, program and validate everything from small devices to complex subsystems to complete systems. Our systems can meet all current cGMP standards and are thoroughly tested. To do this, we observe the highest standards for product and personal safety. When implementing concepts for the pharmaceutical and chemical industries, we work with powerful SCADA systems and control systems such as Siemens PCS7 with and without batch functionality.
For example, we automate the handling of high-quality bulk goods for our pharmaceutical customers worldwide. For automation projects in the GMP/GAMP and CFR21 Part 820 environment, we also work with customers to create the qualification documents required for validation, as well as test plans and test reports in the various phases of qualification: To do this, we comply with qualification processes, e.g. to qualify pharmaceutical manufacturers according to the GMP regulations of the
EU to demonstrate the suitability of your systems for the intended purpose. Qualifications typically start with Design Qualification (DQ), followed by Installation Qualification (IQ) through Functional Qualification (OQ or Operational Qualification) and end with Performance Qualification (PQ or Performance Qualification).
In addition, we also offer engineering and automation services if required. We conceptualize, design, develop, construct, program and validate everything from small devices to complex subsystems to complete systems. Our systems can meet all current cGMP standards and are thoroughly tested. To do this, we observe the highest standards for product and personal safety. When implementing concepts for the pharmaceutical and chemical industries, we work with powerful SCADA systems and control systems such as Siemens PCS7 with and without batch functionality.
For example, we automate the handling of high-quality bulk goods for our pharmaceutical customers worldwide. For automation projects in the GMP/GAMP and CFR21 Part 820 environment, we also work with customers to create the qualification documents required for validation, as well as test plans and test reports in the various phases of qualification: To do this, we comply with qualification processes, e.g. to qualify pharmaceutical manufacturers according to the GMP regulations of the
EU to demonstrate the suitability of your systems for the intended purpose. Qualifications typically start with Design Qualification (DQ), followed by Installation Qualification (IQ) through Functional Qualification (OQ or Operational Qualification) and end with Performance Qualification (PQ or Performance Qualification).