IN THE FIELDS OF LIFE SCIENCES AND THE PRODUCTION OF CHEMICAL RAW MATERIALS, THERE ARE INCREASING DEMANDS ON THE QUALITY AND SAFETY OF PRODUCTS PROCESSED USING BIOTECHNOLOGY. SINCE ASEPTIC PROCESS ENGINEERING IS AN IMPORTANT PART OF ENSURING COST-EFFECTIVENESS AND SAFETY OF THE PRODUCTION PROCESS, IT IS OF GREAT INTEREST TO MANUFACTURERS. TO ACHIEVE CONTAMINATION-FREE PROCESS MANAGEMENT, MANUFACTURERS REQUIRE COMPONENTS USED IN PROCESS ENGINEERING AS WELL AS MEASURING INSTRUMENTS TO COMPLY WITH HYGIENIC DESIGN STANDARDS.

IN TERMS OF PHARMACEUTICAL AND COSMETIC QUALITY REQUIREMENTS, THE STERILIZATION PROCESS IS CRUCIAL TO ENSURE THE PROFITABILITY AND SAFETY OF THE PRODUCT PROCESS. ON THE ONE HAND, IT IS NECESSARY TO STRICTLY IMPLEMENT POLLUTION-FREE OPERATIONS DURING THE PRODUCTION PROCESS, AND AT THE SAME TIME, THE MEASURING EQUIPMENT IN THE PRODUCTION PROCESS NEEDS TO MEET THE HYGIENIC DESIGN STANDARDS.