Oh boiii here we go!!!!
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Oh boiii here we go!!!!
I listen only to my wife.Janoshik, do you listen to Linkin Park? what do you think about Emily Armstrong?
thank you
I can't really tell when I'm being sent a generic and when I'm being sent EU Pharmacopoeia standard / Pharmacy standard / Sample out of pharmacy.i been wondering has there been any generic hgh that tested 99% purity with 0 dimer since changing your testing method?
i see... how much for you to tell me those 5 sources? haha jk wish it was that easyI listen only to my wife.
I can't really tell when I'm being sent a generic and when I'm being sent EU Pharmacopoeia standard / Pharmacy standard / Sample out of pharmacy.
With no label and faked products, how would I know?
We've received EU Pharmacopoeia standard with not label from a client that wanted to test our accuracy.
We've tested 5 samples of GH that were over 99% since we changed our methods.
Hey man I surely appreciate the response!! Everything helps!! I am just trying to figure out what the difference (safety or quality wise) between aas I make and aas made by other labs or even pharmaceutical companies make.. If the solution is sterile, has the correct concentration and has no detected harmful substances.. I dont see any difference. Would you??@dirthand I can't post in that section of the forum, but the most commonly found AAS contamination is:
injectables -> degraded hormone, different hormone, or inert cholesterol based substances
orals -> degraded hormone, different hormone, inert fillers
Hope this helps
Hey, here's a standard certificate of analysis for Pharma Test ester:Hey man I surely appreciate the response!! Everything helps!! I am just trying to figure out what the difference (safety or quality wise) between aas I make and aas made by other labs or even pharmaceutical companies make.. If the solution is sterile, has the correct concentration and has no detected harmful substances.. I dont see any difference. Would you??
Could add in a few positive controls with pharma or compounded pharma products although the absolute concentration of impurities will be lower than in the raws obviously.
1. 3rd party C of A on finished product batch specific to that shipment
- endotoxin screen
- metals with ICP
- purity(ies) / concentration(s) using hplc plus ms (or gcms)
Ok, I am going to start with the simplest example I could think of that may be of interest to members. Getting a C of A from Pharma isn't as easy as it used to be. This took a little work with persistence. I have sanitized some of the details from this one to protect manufacturer confidential information as per forum Terms and Rules.
This is an FDA approved Testosterone Cypionate product manufactured in a large FDA inspected site in Europe operating under USP standards. The manufacturer provides TC to multiple wholesalers who then sell to pharmacies. Will be a decent baseline for...