Quote LOL, "The manuscript of the study (released Sept 28th 2017) will be published next month in the Journal of Clinical Medicine Research. Check the dates buddy "
I don't need to "check the dates" and I'm not your "buddy", as I don't even know you.
Check the dates in the so called "study", and how they "suddenly" cover back to early 2015, up to today. (when has USRM/Comella EVER launched a study/trial and NOT DONE A PR at the start...LIST ONE TIME, ONE?? NEVER HAS HAPPENED, EVER)..this supposed "study" suddenly covers ALL THE SAME PERIOD THE FDA CITED IN 483 INVESTIGATION WARNINGS...and it ain't by "coincidence" if you ask me.
Again, Comella, IMO (it's clearer than crystal to me) is now going to "try" and "claim" that every single patient they "treated" per the FDA "WARNING LETTER" was under some sort of formal "study" (the magic 600 whatever number of patients, will be every patient covered during the FDA investigation time period if you ask me..I'd put bank on it), it's exactly how they "tried" to "claim" the BLIND LADIES were part of a legit and formal "clinical trial" now proven to be 100% FALSE. Same gig, slightly different tactic if you ask me.
It will also allow Comella to "try" and "claim" all the "STEM CELL EXTRACTION KITS" they used (many of which were manufactured at her mother's janitorial supply business, Palm Supply, aka Pavillion Foods inc Florida, Mary Comella owner), that they were all supposedly somehow part of some "research study" blah, blah, blah when they were selling NON FDA APPROVED MEDICAL KITS, also cited in the 483 WARNINGS and the formal "WARNING LETTER", but in redacted form in several places- but the "ENZYME" (aka ADIPOSE, trademarked "CELLASE" or whatever the H they call it) is specifically addressed in the formal warnings, as it's labeled for "RESEARCH USE ONLY" which don't cut it when being used on a invasive surgical procedure on HUMAN PATIENTS.
The FDA has declared that Comella and USCC and thus USRM promote and sell and introduce in to the stream of commerce, an "ILLEGAL DRUG", aka their "SVF PRODUCT" and the "FORMAL WARNING LETTER" says exactly that- it states, "THEREFOR YOUR SVF PRODUCT IS A DRUG". The damn FDA 483 WARNINGS are addressed to... Type of facility: BIOLOGIC DRUG MANUFACTURER
NONE of that is just gonna "blow over" IMO, as is falsely being propagated here and it's not a closed investigation as the FDA has issued no "CLOSE OUT" which must occur, etc. Not a chance in H the FDA is "done" with any of this at this point..no freaking way IMO. CHECK THE DATES....LOL !
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