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
Sustainability and innovation go hand in hand in today’s world, especially in industrial environments where the quality of cleanroom products and environmental considerations are equally important. As part of our commitment to eco-friendly manufacturing, KleanLabs introduces cleanroom doors and components insulated with innovative recycled polyurethane foam, offering cutting-edge solutions that not only meet the highest
Semiconductor clean rooms are vital environments in the microelectronics industry. With properly insulated clean room doors, these spaces are meticulously engineered to maintain extremely low levels of particulates, including dust, airborne organisms, and chemical vapors. The necessity for such cleanliness is driven by the high sensitivity and precision required in manufacturing microelectronic components and semiconductors.
Automotive components are also increasingly expected to be very clean. These demands used to apply to far fewer components, but today the need for cleanliness in the automotive industry is growing exponentially. Ensuring compliance now often requires the use of an automotive clean room to achieve the cleanliness defined by VDA and ISO standards. To
