PFAS Removal Using Ozone-Based AOPs in Pharmaceutical Water
The pharmaceutical industry faces the challenge of having to provide highly purified process water while also meeting requirements for the water’s complete safety. Due to their exceptional persistence and mobility, poly- and perfluorinated alkyl substances (PFAS) pose a particular challenge for industrial water treatment, as conventional physicochemical processes quickly reach their limits […]
Cleanrooms vs. Containment
This presentation highlights the key differences between cleanroom and containment concepts and explains which solution offers the best operational and safety benefits in which situations. It describes fundamental design principles, workflow considerations, and barrier concepts that influence contamination control and operator safety. Participants will gain a clear understanding of how, based on product risk, process layout, and regulatory expectations […]
20 Years of ISPE DACH CU – Who Are We Today?
The ISPE DACH Critical Utilities Organization consists of 21 experts, structured around the three core ISPE areas of Knowledge, Community, and Innovation. Knowledge covers key CU topics such as PW/WFI, pure steam, compliance, gases, automation, monitoring, and microbiology. Community promotes networking through WIP/EL, other CoPs, affiliates, and regulatory agencies. Innovation is responsible for workshops, events, and the organization’s presence at the […]
A holistic approach to project management in the GMP area
Efficient project management in the GMP area is essential for conversions and expansions in existing cleanrooms and in the GMP environment. Companies face numerous challenges, from complying with strict rules and regulations to minimizing business interruptions during the conversion. Ensuring continuous production and ensuring cleanroom classifications are key areas of responsibility. In this presentation [...]
A holistic approach to project management in the GMP area
Efficient project management in the GMP area is essential for conversions and expansions in existing cleanrooms and in the GMP environment. Companies face numerous challenges, from complying with strict rules and regulations to minimizing business interruptions during the conversion. Ensuring continuous production and ensuring cleanroom classifications are key areas of responsibility. In this presentation [...]
A holistic approach to project management in the GMP area
Efficient project management in the GMP area is essential for conversions and expansions in existing cleanrooms and in the GMP environment. Companies face numerous challenges, from complying with strict rules and regulations to minimizing business interruptions during the conversion. Ensuring continuous production and ensuring cleanroom classifications are key areas of responsibility. In this presentation [...]
A holistic approach to project management in the GMP area
Efficient project management in the GMP area is essential for conversions and expansions in existing cleanrooms and in the GMP environment. Companies face numerous challenges, from complying with strict rules and regulations to minimizing business interruptions during the conversion. Ensuring continuous production and ensuring cleanroom classifications are key areas of responsibility. In this presentation [...]
A holistic approach to project management in the GMP area
Efficient project management in the GMP area is essential for conversions and expansions in existing cleanrooms and in the GMP environment. Companies face numerous challenges, from complying with strict rules and regulations to minimizing business interruptions during the conversion. Ensuring continuous production and ensuring cleanroom classifications are key areas of responsibility. In this presentation [...]
Cleanrooms and Fire Safety – How Do They Go Together?
From the perspective of many planners and users, cleanroom technology, building code requirements, and occupational safety do not go hand in hand. At first glance, the stringent hygiene requirements for cleanrooms in research, manufacturing, and healthcare seem very difficult to reconcile with the regulations for a “standard building.” This presentation highlights possibilities and examples of how the high hygiene […]
Energy-efficient cleanrooms start with the planning phase
The presentation explains why energy-efficient cleanrooms must be considered from the early planning stages and why estimates or SOP guidelines are not a suitable basis for precise design. Cleanrooms have significantly higher energy requirements compared to unclassified areas, which is why data-driven planning is essential. A key factor here is the correct determination of the air cleanliness class in accordance with ISO 14644 and […]