pharmaceutical industry
Pharmaceutical Engineering
Whether small devices or complete systems – from prototype construction to series production, you can rely on us
Our specialists manufacture to the highest quality standards. In addition, we offer engineering and automation services as needed. We conceptualize, design, develop, construct, program, and validate everything from small devices and complex subsystems to complete plants. Our systems meet all current cGMP standards and undergo rigorous testing. We adhere to the highest standards for product and personnel safety.
When implementing concepts for the pharmaceutical and chemical industries, we work with high-performance SCADA systems and control systems such as Siemens PCS7 with and without batch functionality. For example, we automate the handling of high-value bulk materials for our pharmaceutical clients worldwide.
For automation projects in GMP/GAMP and CFR 21 Part 820 environments, we collaborate with clients to create the required qualification documents, test plans, and test reports for validation in the various phases of qualification.
We adhere to qualification processes, for example, to demonstrate the suitability of pharmaceutical manufacturers' systems for their intended purpose in accordance with EU GMP regulations. Qualifications usually begin with the design qualification (DQ), followed by the installation qualification (IQ) up to the functional qualification (OQ or “Operational Qualification”) and end with the performance qualification (PQ or “Performance Qualification”).
When implementing concepts for the pharmaceutical and chemical industries, we work with high-performance SCADA systems and control systems such as Siemens PCS7 with and without batch functionality. For example, we automate the handling of high-value bulk materials for our pharmaceutical clients worldwide.
For automation projects in GMP/GAMP and CFR 21 Part 820 environments, we collaborate with clients to create the required qualification documents, test plans, and test reports for validation in the various phases of qualification.
We adhere to qualification processes, for example, to demonstrate the suitability of pharmaceutical manufacturers' systems for their intended purpose in accordance with EU GMP regulations. Qualifications usually begin with the design qualification (DQ), followed by the installation qualification (IQ) up to the functional qualification (OQ or “Operational Qualification”) and end with the performance qualification (PQ or “Performance Qualification”).