readalot
Member
Very early to make any conclusions. From a statistical standpoint we simply don't have sample size to draw any meaningful conclusions.I say this because have you seen any concern with anything that’s been tested that way? I will say I am a fan of the sterility test even though it really is only representing the single vial that was tested.
Jano did mention some failed tests but until we can get some type of surveillance database with "events" we don't know. Hence I was trying to get him to anonymize results and report quarterly numbers on peptides and finished oils.
I simply state: a passing test is not a wasted test. Surveillance is a continuous process. Don't crash the plane before it takes off. Collect the data and in a year you can all tell me "told ya so". There's also the not so small details around endotoxin calibration with oils.