Sterilization is a process to make products free from viable microorganisms. Some semi - critical and all critical medical devices should be sterilized before next use. Reference standards include FDA guidance, AAMI TIR 12: 2020, ISO 17664 - 1: 2021 and others. Sterilization effi......
FDA recommends package test methods include simulated distribution and aging followed by associated packaging testing to demonstrate packaging materials can maintain sterile barrier integrity during device shelf - life. Device - specific performance testing for storage effects is......
The Clinical Trial Team offers comprehensive services for clinical trials of Class II, III and innovative medical devices. Services include protocol design (trial protocol, informed consent form etc.), clinical monitoring (site screening, ethical communication etc.), data managem......
The expert team of EPIN Medical Device Animal Experiment Center has been involved in medical device animal test research since the 1990s and is among the earliest in China to learn FDA animal tests and evaluations. The EPIN Large Animal Experiment Center covers about 5000㎡, with ......