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The need for contaminant-free spaces in order to support essential research and production activities in Life Sciences industries makes pre-engineered cleanrooms a suitable solution for many. These specialized facilities are designed to provide controlled environments with minimal airborne particles, ensuring the integrity of critical processes in biotechnology, pharmaceuticals, and other life sciences fields.
By immersing ourselves in this crucial sector over the years, we now have the capacity to support companies in providing quality cleanrooms according to all customer requirements. But we also offer support in the areas of personnel training, gowning processes and environmental monitoring.
Pre-engineered cleanrooms play a vital role in the Life Sciences industries, providing controlled environments for manufacturing, testing, and research activities.
Our cleanrooms are designed and built using standardized modules and components, which offer various advantages over traditional construction methods. In this way, we can ensure the integrity and quality of pharmaceutical products.
ISO or cGMP
The primary purpose of a cleanroom is to control and minimize contamination. Our cleanrooms are classified according to the cGMP or ISO standards (ISO 14644-1).
Temperature & humidity control
Precise control of temperature and humidity is essential to maintain product stability and reproducibility of results, especially in pharmaceutical manufacturing and biological research.
Pressure differentials
Maintaining specific pressure differentials between cleanrooms and adjacent spaces prevents cross-contamination by ensuring that air flows from cleaner areas to less clean areas.
Materials & equipment
Cleanroom materials, including surfaces, furnishings, and equipment, must be compatible with the cleanroom environment. Non-shedding, non-reactive, and easy-to-clean materials are preferred.
All equipment used in the cleanroom must be appropriately qualified and calibrated to ensure accurate and consistent results. Validation processes are crucial.
Gowning
Strict gowning procedures, including the use of sterile clothing, gloves, and head coverings, are enforced to prevent personnel-generated contamination.
Cleanrooms in life sciences require thorough validation and qualification processes to demonstrate compliance with regulatory requirements and industry standards.
Continuous monitoring of environmental conditions, such as temperature, humidity, particle counts, and pressure differentials, is essential. CleanConnect, our data logging and reporting systems ensures 100% traceability and compliance.
The need for contaminant-free spaces in order to support essential research and production activities in Life Sciences industries makes pre-engineered cleanrooms a suitable solution for many. These specialized facilities are designed to provide controlled environments with minimal airborne particles, ensuring the integrity of critical processes in biotechnology, pharmaceuticals, and other life sciences fields.
By immersing ourselves in this crucial sector over the years, we now have the capacity to support companies in providing quality cleanrooms according to all customer requirements. But we also offer support in the areas of personnel training, gowning processes and environmental monitoring.
Pre-engineered cleanrooms play a vital role in the Life Sciences industries, providing controlled environments for manufacturing, testing, and research activities.
Our cleanrooms are designed and built using standardized modules and components, which offer various advantages over traditional construction methods. In this way, we can ensure the integrity and quality of pharmaceutical products.
ISO or cGMP
The primary purpose of a cleanroom is to control and minimize contamination. Our cleanrooms are classified according to the cGMP or ISO standards (ISO 14644-1).
Temperature & humidity control
Precise control of temperature and humidity is essential to maintain product stability and reproducibility of results, especially in pharmaceutical manufacturing and biological research.
Pressure differentials
Maintaining specific pressure differentials between cleanrooms and adjacent spaces prevents cross-contamination by ensuring that air flows from cleaner areas to less clean areas.
Materials & equipment
Cleanroom materials, including surfaces, furnishings, and equipment, must be compatible with the cleanroom environment. Non-shedding, non-reactive, and easy-to-clean materials are preferred.
All equipment used in the cleanroom must be appropriately qualified and calibrated to ensure accurate and consistent results. Validation processes are crucial.
Gowning
Strict gowning procedures, including the use of sterile clothing, gloves, and head coverings, are enforced to prevent personnel-generated contamination.
Cleanrooms in life sciences require thorough validation and qualification processes to demonstrate compliance with regulatory requirements and industry standards.
Continuous monitoring of environmental conditions, such as temperature, humidity, particle counts, and pressure differentials, is essential. CleanConnect, our data logging and reporting systems ensures 100% traceability and compliance.
Legolisation means standardisation. Standardisation causes a shift in production. Work is carried out in conditioned spaces such as factory halls. our cleanrooms are manufactured partly or entirely off-site, which means huge savings on transport costs and reduction of inconvenience on-site