Cleaning Evaluations of Newly Manufactured Devices

With the implementation of 19227:2018 Implants for surgery - Cleanliness of orthopedic implants - General requirements, evaluation of residual levels after the final manufacturing process has become a regular expectation from both OEM customers and regulatory bodies. However, determining a test strategy based on the device use remains a challenge for many. Learn about cleaning validations for newly manufactured devices and considerations for devices outside the scope of ISO 19227. This webinar will focus on the cleaning validation plan from identification of potential contaminants, to test strategy, and evaluations of results.