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Factors Influencing Individual GHK-Cu Results and Common Protocol Errors Two individuals following the exact same GHK-Cu protocol might experience different outcomes

or Appears on the 503A bulks list or 503A Category 1 Bulk Drug Substances Under Evaluation list (i.e., the interim 503A bulks list) provided by the FDA if requirements one or two are not met *note that the FDAs position is that specifically refers to USP/NF drug monographs, not dietary supplement monographs 503B outsourcing facilities are even further restricted in their allowed bulk materials and may not compound a drug product unless the relevant bulk drug product, in addition to being accompanied by a valid CoA and manufactured in an FDA registered facility, meets one of the below requirements: Appears on the list identifying bulk drug substances for which there is a clinical need (503B bulks list or 503B Category1: Bulk Drug Substances Under Evaluation (i.e., the interim 503B bulks list)

If the FDA moves these peptides to the 503A Bulks List, it doesnt mean that they are approved as drugs

Yet, because of its susceptibility to the actions of proteolytic enzymes it is important to ensure its sustained delivery in bioactive concentrations

Inconsistent results Inconsistent response usually indicates inconsistent administration