Safe cleanroom operation with a monitoring system
We will take you with us and show you what is important when planning, implementing, operating and optimizing a holistic cleanroom monitoring system. You will gain practical insights, an overview of the most important stages and we will show you why the life cycle should play a role right from the planning stage. Regardless of whether you are [...]
Training 4.0 - Creating understanding with virtual reality
The hybrid concept combines theory, practice and VR in the Osnabrück cleanroom training center. Certified trainers provide practical training for specialists and managers, supported by VR technology to optimize movements and visualize air and particle flows. In the train-the-trainer program, managers are comprehensively trained in order to provide employees with targeted and practical training. This ensures a sustainable transfer of knowledge, standardized training and optimal preparation.
Microbiological control of pharmaceutical water
Water is one of the most important media in the pharmaceutical industry. Due to the wide range of applications of water in pharmaceutical production, its microbiological control is of great importance. During the lecture, water as a possible source of contamination in pharmaceutical production will be explained in more detail and the regulatory requirements for microbiological water control will be discussed. The lecture provides an [...]
VI: Test sets as the basis for the threshold study
The importance of visual inspection in the pharmaceutical industry, particularly with regard to quality assurance and the improvement of inspection processes. Important topics are: Defect catalog: A list of possible defects that serves as a basis for inspection and enables a standardized assessment. Threshold study: Definition of threshold values for the detection of product defects to ensure that inspection systems and personnel work reliably. [...]
Sustainability & decarbonization in the pharmaceutical industry
Sustainability and decarbonization are key strategic issues not only for Siemens. Given the complexity of decarbonization in the pharmaceutical industry, it is necessary to use all available options to reduce CO2 emissions at a site. The key areas here are: > Optimization of ancillary facilities and site infrastructure > Design and operation of the energy system > Process design [...]
Cybersecurity in pharma: holistic with the B3S standard
Cybersecurity is essential for operations, especially in the pharmaceutical industry. In light of increased threats, existing security measures need to be reconsidered. Laws and guidelines such as B3S, NIS2 and KRITIS provide guidance for cybersecurity, but allow flexibility for practical implementation. The cybersecurity process begins with the identification of vulnerable assets, followed by the implementation of physical, technical and organizational measures. It is important [...]
Cleanrooms: Planning & optimization with 3D simulation
By using the latest 3D CAD tools and flow simulations, you can create a digital twin of your cleanroom that provides a precise basis for planning and optimization. This innovative technology enables you to design new cleanrooms efficiently or adapt existing cleanrooms in a targeted manner. In the virtual design, potential weak points can be identified and rectified at an early stage, which not only [...]
Cleanroom applications for the sterile area
Customized stainless steel equipment for laboratories and the pharmaceutical industry Manufactured in Germany according to GMP guidelines. Under the Müller ReinRaum brand, Müller Feinblechbautechnik GmbH has been selling customized stainless steel products for the pharmaceutical industry since 2012. We have over 25 years of experience in the field of laboratory and cleanroom equipment. The advantages of Müller [...]
OSD Production
Maintaining strict health and safety standards in pharmaceutical production while meeting regulatory quality requirements. Pharmaceutical manufacturers are increasingly looking for ways to reduce production costs while improving safety and quality. Cleanroom air filtration and process dust capture solutions are critical to ensuring the manufacture of high quality pharmaceutical products [...].
Leaks in pharmaceutical production: Discard the product?
Leaks during manufacturing are unfortunate, but a reality in pharmaceutical production facilities that use single-use technology. They pose a risk to product quality and safety due to the possibility of contamination. A final risk-based assessment is used to decide whether a batch should be further processed or discarded. As it is not possible to fully prove that no contamination [...]