Cleanroom cleaning: From the general to the specific
Standards and guidelines are essential components in the cleaning of a cleanroom, but how do we implement them correctly in daily use? It is obvious that there is a wide range of tools and aids for carrying out cleaning and disinfection measures. But which equipment should be used when, where exactly the advantages lie and [...]
Support for the CCS (Contamination Control Strategy)
Supporting the CCS (Contamination Control Strategy) through metrological testing and verification What does a CCS involve - how can it be supported/implemented metrologically? How does cyclical cleanroom qualification fit into the concept and what are the findings? What can flow visualization contribute and what needs to be considered? What needs to be considered for calibration & mapping [...]?
Filtration technology for production processes in cleanrooms
This presentation will discuss contamination control in cleanrooms, highlighting the challenges in the various process steps in relation to HEPA and AMC filtration. Process safety and risk management are the key success factors for efficient processes and product reliability. Product contamination is not only problematic and costly - it also damages reputation and image and delays [...]
Top down cleaning
Regular top-down cleaning is essential for the operation of a cleanroom. The presentation will therefore first explain what top-down cleaning is. Furthermore, the advantages, the necessity and the requirements for carrying out a top-down cleaning are explained.
AdvantaPass - Fluid transfer in cleanrooms with wall-through
AdvantaPass® - Clean Room Pass Through Technology Cleanroom wall portal for customized single-use systems AdvantaPass is a patented system that enables the aseptic transfer of liquids between rooms in pharmaceutical production facilities. The system provides complete separation between different cleanroom classes when transferring liquids. AdvantaPass offers a practical, safe and easy way to transfer large volumes of liquids from room to room [...]
Planning a qualification in the pharmaceut. industry
This webinar is about how GMP-compliant qualification of pharmaceutical plants is carried out. We will explain why it is important to qualify production facilities and to document this in a GMP-compliant manner. You will receive helpful tips on what is important for an audit. The knowledge imparted will enable you to optimize your processes and audit preparations, reduce production costs and improve product quality [...].
Planning a qualification in the pharmaceut. industry
This webinar is about how GMP-compliant qualification of pharmaceutical plants is carried out. We will explain why it is important to qualify production facilities and to document this in a GMP-compliant manner. You will receive helpful tips on what is important for an audit. The knowledge imparted will enable you to optimize your processes and audit preparations, reduce production costs and improve product quality [...].
World's first germ collection head with integrated agar
The BioCapt® Single-Use cleanroom airborne microbial monitor helps minimize false positives for airborne microbial activity in cleanrooms for pharmaceutical applications by reducing contamination introduced during the handling of sedimentation plates. This avoids time-consuming investigations and increases production. In addition, many expensive and time-consuming sterilization steps such as autoclaving, disinfection and the associated handling and [...]
Particle contamination in high-purity liquids
Continuous monitoring of particles in fluid systems provides valuable real-time data that allows us to identify and eliminate sources of particle contamination. Understanding the data generated by the particle counter plays a key role in this. This webinar will cover a range of useful data analysis techniques that can be applied to data from liquid particle counters. It starts with basic techniques such as the [...]
Fundamentals and development trends of filter fan units (FFU)
The presentation deals with the basics of filtration in cleanroom technology. It discusses the structure of modern cleanrooms and presents possible designs of cleanrooms with filter fan units. The correct dimensioning of the FFU is the success criterion for high production reliability. Issues such as noise emissions, compliance with the required cleanroom classes and energy consumption have a major influence on successful [...]