QSI has announced that the Instrument Validation Module has been included in the latest WinLIMS software release, tool currently available for ensuring the quality of analytical data provided by the ...
Compliant documentation in the drug manufacturing process is essential. 21 CFR Part 11 compliance software helps achieve this from raw materials to finished goods. In addition, the qualifications of ...
The correlation between swab assay results and visible-residue limits (VRLs) for cleaning validation was examined. Previously completed validation studies were reviewed to compare swab results with ...
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