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A Data-Derived Approach For Selecting Criticality Levels In FMECAs For Cleaning Process Risk Analysis

Revision Of The ASTM E3263 Standard For Visual Inspection Of Pharmaceutical Manufacturing Equipment And Medical Devices For Residues

ASTM has published the revision of ASTM E3263 "Standard Practice For Qualification Of Visual Inspection Of Pharmaceutical Manufacturing.

How political action committees transformed school board races in Round Rock and Leander

Political action committees don't typically get involved in local school board races. But money and endorsements from local, state and national PACs ultimately helped determine the results of school board races in Round Rock and Leander.

Calculating Process Capability Of Cleaning Processes With Completely Censored Data

Data below the detection limit (DL) are known as left-censored data. Quite often, 100% of the results of the cleaning samples fall below the DL. How.

Replacing The MACMACO With The MSC Rethinking How Cleaning Validation Limits Are Calculated

Two of the most commonly used terms used in pharmaceutical cleaning validation are the Maximum Allowable Carryover (MAC or MACO) and the Maximum Safe.