Reducing CO2 and energy consumption in HVAC systems
This presentation describes the growing importance of sustainability in the pharmaceutical industry. It begins with an analysis of energy consumption in HVAC systems at production facilities and then presents specific case studies and design principles. The presentation highlights several ways to reduce energy consumption and CO₂ emissions, including measurable upgrades. It also emphasizes how the design of HVAC systems can help stakeholders […]
Life cycle assessment in ventilation and air-conditioning technology
This presentation examines the methodology for determining the ecological footprint of HVAC systems. Using the example of an HVAC system for a pharmaceutical production and filling line, it demonstrates how smart technologies open up new avenues for greater sustainability. Findings from a life cycle assessment show that the operational phase of these HVAC systems has an even greater impact on overall efficiency than […]
How to Ensure Hygiene and Reduce Operating Costs
Air handling systems play a crucial role in maintaining cleanroom hygiene. This presentation demonstrates how careful planning and design enable air handling solutions that meet strict hygiene standards while operating efficiently—thereby providing clean air with minimal resource consumption.
Rethinking Learning: How to Build Lasting Skills
In the context of cleanrooms, employee training is a requirement under GMP regulations—but does it actually make a difference? In this presentation, we’ll explore how companies can design learning experiences that not only impart knowledge but also develop skills and ensure they’re actually applied in day-to-day work. The first part of the presentation will discuss modern learning architectures such as microlearning or […]
GMP non-compliance in the tension between quality, cost, and time
Based on many years of consulting experience, certain GMP issues frequently arise in the manufacture of healthcare products. These issues are examined in detail, along with proven countermeasures and ways to mitigate deficiencies. Underestimated GMP deficiencies can quickly become a threat to the very existence of companies in the GXP sector—but this does not have to be the case. At first glance, it is surprising that certain […]
Humidity as a Key Factor in Cleanrooms
Controlling humidity in cleanrooms is a key factor in ensuring stable production processes and compliance with quality standards. The presentation will explore the technical fundamentals of air humidification, typical challenges such as particle prevention and hygienic design, as well as integration into existing ventilation and HVAC systems. Using practical examples, various solution approaches will be presented that focus on energy efficiency, operational reliability, and standard-compliant design […]
Validation of an RMM for pharmaceutical water
Alternative methods for microbiological monitoring offer significant advantages over conventional plate testing. However, none of these alternative methods have yet been validated for pharmaceutical water. In this presentation, we will walk you through all the procedures and steps required for successful validation. Once validated, alternative methods can be used not only for in-process control but also for quality control. This means […]
Innovative Solutions for CERN
In addition to cleanroom technology and the resulting requirements for ambient air, “clean” cooling is also becoming increasingly important in building services engineering. Alongside the impact of the EU’s F-Gas Regulation, a growing segment of the population is becoming aware of the environmental risks associated with the continued use of PFAS, HFO, and TFA. The […]
Online microbial monitoring using flow cytometry
Alternative methods for monitoring microbial contamination in pharmaceutical water have been sought for many years, and various technologies are now available on the market. Each method has its own specific advantages and disadvantages. In this presentation, we will demonstrate examples of the use of flow cytometry as a microbiological monitoring tool for pharmaceutical water. Continuous monitoring enables the application of trend rules to the process data. […]
Room Monitoring in Practice: Compliant, Precise, Transparent
Focus on Cleanrooms – Best Practices for Monitoring: How Does ELPRO Do It? • Combining Room Parameters and Particles • Fixed Sensors Plus Mobile Sampling • Sensor and Measurement Module Placement • Integrating Device Sensors into the CMS • Different Setups by Zone and Class: Variety and Typical Setups—What Can Be Measured? What Makes Sense? There are various […]