
Originally Posted by
MuscleInk
The Food and Drug Association requires that any and all drugs designated for human consumption must undergo four phases of clinical research testing under an IND protocol and once the safety and efficacy if each drug is proven, submitted for FDA approval under an NDA.
Drugs sold by most of these research chem companies such as Ar-r are biosimilar or bio equivalent compounds of drugs already approved so the vendor (Ar-r) in this case is copying approved drugs. They could NOT recommend use in humans without proper clinical testing even though they are copies of other approved drugs, so by law, Ar-r and other research chem companies MUST label their compounds with the disclaimer, "Not approved for human use. For research purposes only".
Many of the compounds sold and used and used in steroid cycles which are ILLEGAL drugs and the ancillaries we use have not been tested for efficacy and safety even though the mechanism of action is known.
For example, the liquidex sold by Ar-r is a biosimilar of Anastrozole. Even though liquidex is bio equivalent to the real Anastrozole it could not be prescribed for human use until it is tested in a four phase clinical trial.
Make sense?