What if the core of a cleanroom door didn’t come from newly produced materials, but from an old cold room or a wall panel? We at KleanLabs® joined forces with Purman® to execute this objective to the highest standard. The two Central European companies developed an industrial-scale recycling method that gives end-of-life PU/PIR foams a
Maintaining the highest levels of cleanliness and preventing cross-contamination are paramount in the world of controlled environments. Cleanrooms depend on precise regulation of temperature, humidity, and airborne particles to protect product integrity and process reliability. A key component in these systems is the cleanroom pass-through box – an essential tool for safely transferring materials in
Pass-through chambers (also called pass-through boxes) have become a ‘must’ in many industries over the years. When creating a production process, material flow must be designed in accordance with the various standards the lab must comply with. Two environments in the same lab might have very different hygiene requirements that must be taken into consideration
Pharma clean rooms are critical for protecting products and ensuring compliance. In this guide, you’ll learn the key clean room requirements for pharmaceuticals, ISO classifications, design best practices, and common mistakes to avoid. We’ll also cover new technologies that make clean rooms smarter and more efficient. Requirements and standards for pharmaceutical clean rooms Regulatory compliance
