WestPack 2023 Answers Your Packaging Education Questions
Leading organizations contribute to the strength of the packaging education offered at our early-February show in Anaheim, California.
Source: packagingdigest.com
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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...
Source: meddeviceonline.com
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...
Source: pharmaceuticalonline.com
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...
Source: pharmaceuticalonline.com
Calculating Process Capability Of Cleaning Processes With Partially Censored Data
When cleaning sample results are below the detection limits (DLs) of an analytical method, these data are known as "non-detects" or...
Source: pharmaceuticalonline.com