ZHYQ’s best practice of sterile process engineering adds to the profitability and safety of the manufacturing system. Additionally, sterile process engineering may ensure compliance to the validation process within all sanitary approval agencies.
A process flow that is free of contamination requires peripheral components such as pressure and temperature measuring instruments to ensure that the process parameters are within allowable limits.
ZHYQ's instrumentation meets or exceeds the stringent requirements of approval agencies and conforms to GMP (Good Manufacturing Practice) guidelines.
Tel: +86-21-67755188 67755189 Fax: +86-21-67755185 E-mail: firstname.lastname@example.org