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Introduction To ASTM E3263-20 Standard Practice For Qualification Of Visual Inspection Of Pharmaceutical Manufacturing Equipment And Medical Devices For Residues


Introduction To ASTM E3263-20:
By Andrew Walsh, Ralph Basile, Ovais Mohammad, Stéphane Cousin, Mariann Neverovitch, and Osamu Shirokizawa
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Visual inspection has been widely used for many years by the pharmaceutical, biologics, and medical device industries after cleaning to release manufacturing equipment and devices. However, visual inspection has never been demonstrated to be an effective, reliable, or safe method to use for these inspections. Recently, the European Medicines Agency (EMA) issued a Q&A
1 to its guideline on determining health-based exposure limits (HBELs) that describes what criteria have to be met for visual inspection to be acceptable to the EMA for release of manufacturing equipment. Some form of guidance or a standard has been needed to guide these industries on how to meet these criteria and demonstrate that operators/QA inspectors are capable and qualified to accurately assess the absence or presence of residues on m ....

United States , United Kingdom , Ester Lovsin Barle , Miquel Romero Obon , Andreas Flueckiger , Davidg Dolan , Gabriela Cruz , Ioana Gheorghiev , Igor Gorsky , Prakash Patel , Zimmer Biomet , Robert Kowal , Mallory Degennaro , Vander Weilen , Stephen Spiegelberg , Delane Dale , Andrew Walsh , Spiro Megremis , Bristol Myers Squibb , Rodney Parker , Van Nostrand , Michel Crevoisier , Thomas Altmann , Sarra Boujelben , Norma Turner , Mariann Neverovitch ,