Readalots Enhanced Testing

demanding a higher testing standard that quantifies the presence of bacteria in UGL gear, which will be present, even if at a low level, unless terminal sterilization is used, and, endotoxin testing, which despite insistence its "irrelevant" (it's not in terms of long term health) , the tiniest compounding pharmacies check for all their injectable products.

Excellent comments. As you can see above we are doing endotoxin screen this go around on the raw along with the other stuff. I don't have a good solution yet for adequate class 1 and 2 residual solvents.

What testing do you want to see on next go around?

Makes no sense to do sterility on a raw that will get filtered but down the road what would you like to see on the finished oil products WRT terminal sterilization angle. My thinking is some endotoxon screens on finished products after we get some data on baseline for raws. Unsure of the oil quality landscape for the UGLs. Would have to be some pretty nasty oil for LPS coming from the carrier oils?

Background for folks...

 
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QSC GH sterility result (Jano, July 2024 from Discord Group; thanks Discord Group!).

Cross reference.

Appears there is no regular/routine testing for the batches from the vendor for sterility.

 
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