Biopharmaceutical water purification equipment system has some special requirements for fittings and instrumentation:
Material selection: fittings and instrumentation should be in line with the relevant standards of the biopharmaceutical industry, usually requires the use of 316L stainless steel or other special alloys to meet the requirements of the material to ensure that it is corrosion-resistant and high-temperature resistant.
Surface smoothness: The inner surface of the fittings and the surface of the instrumentation should have a certain degree of smoothness, in order to reduce the possibility of microbial growth and adhesion, to avoid contamination of the production process.
Sealing: the interface of the pipe fittings and the connecting part of the instrumentation should have good sealing performance to ensure the stable operation of the water system and avoid the water quality being polluted by the outside world.
No dead-end design: the design of the fittings should try to avoid dead ends or areas that are difficult to clean for effective cleaning and disinfection.
Compliance with GMP requirements: All fittings and instrumentation should comply with the relevant requirements of Good Manufacturing Practice (GMP) to ensure the quality and safety of the production process.
Preventing leakage: The connecting parts of fittings and instrumentation should be designed to prevent leakage in order to avoid contamination of the water quality of the purified water system.
Easy to maintain and service: Fittings and instrumentation should be easy to maintain and service to ensure stable operation and long-term reliability of the system.
Please note that specific requirements may vary depending on factors such as production process, product type, etc. Therefore, it is best to consult with a professional engineer or follow the appropriate industry standards and codes when selecting and designing fittings and instrumentation.