This webinar will provide valuable guidance to medical device manufacturers on how to establish and justify limit values for cleanliness. There are several techniques that may be used to set these limits, including comparison involving statistics and historical data. Justification techniques include biocompatibility and risk assessment. Regardless of what technique is used, regulatory agencies expect that limit values will be set for residual analysis.
Scheduled On : Monday, December 9, 2013 at 13:00 Hrs
Scheduled On : Monday, December 9, 2013 at 13:00 Hrs
