Streamline your path to purity: Optimize your production with efficient cleanroom design.
SYNTEC AIRFLOW SYSTEMS has been in the business of designing, engineering, and executing cleanroom projects for various life science and healthcare applications for several decades. Our expertise includes containment and Bio-Safety level (BSL1, BSL2, BSL3, BSL4) facilities. Thanks to Our in-depth knowledge of processes, medical planning, various regulatory guidelines, and GMP requirements, SYNTEC is the ideal partner for designing and engineering cleanroom solutions.
In order to achieve Good Manufacturing Practice (GMP) cleanrooms, SYNTEC follows the International Society for Pharmaceutical Engineering (ISPE) guidelines, unless otherwise required by the client. We are thoroughly familiar and extensively use GMP regulations such as EU GMP, USFDA, WHO, PICs, and cGMP etc.
SYNTEC offers different cleanroom partition systems design that can be adapted to a variety of cleanroom requirements based on the usage of the cleanroom. The selection of the cleanroom partition system is done according to the usage, environments, fire protection, heat preservation, noise reduction, moisture proof, etc.
The high-level design ensures the excellent function and appearance of the cleanroom, providing modular construction but integrated solution. At SYNTEC, the architecture and engineering department consists of highly qualified professionals who put in all the necessary efforts to deliver high-quality cleanroom design and engineering.
For particle-based cleanliness, SYNTEC mostly follows the ISO 14644 standard. Cleanrooms and associated controlled environments provide for the control of airborne particulate contamination to levels appropriate for accomplishing contamination-sensitive activities.
