february 19, 2014 webinar
noon - 1:30 pm eastern standard time
cleaning validation is a key part of pharmaceutical, biopharmaceutical, and medical device manufacturing. one of the critical steps in performing a successful cleaning validation is establishing the limits of residue that can remain on the surface being cleaned. several factors can impact the selection and validation of these residual limits, such as sampling technique, analytical methodology, and areas of non-uniform contamination.