Aseptically safe: cleaning in critical areas

Maintaining aseptic conditions in Class A environments—such as isolators, restricted access barrier systems (RABS), and biological safety cabinets (BSCs)—requires strict cleaning and disinfection protocols. This presentation explains the regulatory requirements for cleaning and disinfection in Class A areas. Taking these requirements into account, best practices for cleaning surfaces within the aseptic core area, including the […]

Introduction Hygienic Design

Die Präsentation erläutert Hygienic Design als ganzheitliche konstruktive Gestaltung von Anlagen und Umfeld, um sichere Lebensmittel zu gewährleisten. Zentrale Elemente sind reinigbare Konstruktionen, geeignete Werkstoffe, Fremdkörpervermeidung, gute Wartbarkeit und klare Zonenkonzepte. Die fünf Kernthemen umfassen Fabrikgestaltung, Versorgungssysteme, reinigungsgerechte Apparate, Reinigungs- und Desinfektionsprozesse sowie Personalhygiene. Hygienic Design reduziert Risiken wie Kontamination, Rückrufe und Kosten, verbessert Produktqualität […]

Planning Material Flow and Intralogistics in a GMP Environment

Planning material flow and intralogistics in a GMP environment places high demands on the layout—particularly due to hygiene zones, airlocks, and the need to prevent cross-contamination. This presentation demonstrates how these factors influence material flow and intralogistics, and which solutions can help combine efficiency and compliance as early as the concept design phase. Modular planning and automated transport systems enable […]

Hardware and Software Solutions for Climate Monitoring

Modular software for measurement technology with over 40 years of market presence across many industrial sectors. The range of services extends from small-scale testing tasks to extensive monitoring tasks in the pharmaceutical industry, test benches, production, certification bodies, aerospace, and the automotive industry. MCPS is not a programming or development tool. The average end user can quickly and effectively configure and perform their measurement tasks. In […]

Introduction of a mobile decontamination system

The filling of a powdered antibiotic, a process that has been carried out for decades, takes place in a RABS within a cleanroom. The previous method of formaldehyde fumigation was no longer up to date, so alternatives were sought. These were found in H₂O₂ decontamination, with the aim of both keeping costs low and avoiding extensive structural modifications. This presentation covers […]

Professional HVAC maintenance in accordance with VDMA 24186

This presentation explains why proper HVAC maintenance in accordance with VDMA 24186 is crucial for maintaining stable cleanroom conditions—because if the air stops moving, the cleanroom stops functioning. The presentation covers the relevant maintenance steps for supply air, exhaust air, and recirculation systems, the condition of critical components such as filters, fans, and humidifiers, as well as typical weak points that can compromise the cleanroom. It also explains how […]

Flawless hygiene inspection in accordance with VDI 6022 in cleanroom facilities

This presentation provides a concise overview of how to properly conduct a hygiene inspection of cleanroom HVAC systems in accordance with VDI 6022. It covers the specific hygiene requirements in controlled environments, key inspection steps, and the evaluation of sensitive components such as filters, humidifiers, and air distribution systems. In addition, it identifies common sources of error in cleanroom practice and explains how to reliably avoid them. […]

Forward Thinking: The Future of Glove Manufacturing

Innovation doesn’t always mean reinventing the wheel. Sometimes it’s about refining simple ideas that have stood the test of time. This presentation shows how the evolution of gloves—from the earliest forms of protection to modern insulated gloves—demonstrates the enduring power of practical thinking. We explore how traditional concepts continue to drive modern advancements […]

Quick In – Quick Out: Loading and unloading—but the smart way!

When discharging material from GMP class "B" to "E", it was previously necessary to carry out 3 airlock processes - one for each GMP class. This costs a lot of time and personnel. With the BECKER QuickOut ® airlock, this is now possible in just one step: thanks to an internal two-chamber principle with integrated chute, there is no longer any risk of [...]

Designing, Building, and Operating Energy-Efficient Cleanrooms

Hardly any other term has developed as much in recent years as the term "sustainability". But what does sustainability actually mean and what does it have to do with cleanroom technology? First and foremost, it means using existing resources sparingly and reducing the CO2 footprint, especially with regard to climate change. The presentation will [...]