Why would they test the same product again? They test it by a TGA approved lab, they get the result they need, they release it.
Another TGA lab gets a different result...
Things do not change over time, I am unsure what you are basing that on. If that were the case, all medicine would be useless. That would mean they could sell a bottle to a customer, and a month later it no longer has the concentrations that have been medicinally approved??
I imagine their testing requirements are per production/batch - and the results were well within the requirements as mentioned. There is a problem with either one of the approved labs (from what I am reading), I am not sure what else could be done aside from ultra-paranoid, expensive re-testing of everything, which could most likely yield the initial results?
Am i missing something here?
Ann: TGA Medicinal Cannabis Post Market Survey, page-12
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