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Re: Simpsonly post# 163257

Tuesday, 12/04/2018 9:57:25 AM

Tuesday, December 04, 2018 9:57:25 AM

Post# of 334351
Takes no responsibility at all, they make it sound like it's just a matter of resubmitting. Were they asleep May 9th during the presubmission meeting? Why wasn't this revealed after that meeting.

Never says BOO about allowing Bayer to have access for way to long only to blatantly put that product up for sale. An OBVIOUS Slap to out face, showing us ZERO respect.

You bet I know when, and it AIN'T any time soon. More evidence that he's in way over his head, and it didn't sound like he's going to tap GP on the shoulder for help.

That's the part that speaks volumes to me, they cant get past the FDA without GP navigating us thru IMPOSSIBLE TERRAIN. They are much more experienced at dealing with the FDA. Prior to the previous two clearances back in 2/17, GP was helping us get approval after the FDA had reclassified the product into a brand new classification. Apparently the FDA still doesn't understand PEMF, and thinks they can continue to bleed the money we invest in a trial and error game of submissions. Time lost is the l
part that really bothers me. An entire year gone with ABSOLUTELY ZERO TO SHOW FOR IT.

The FDA is the bodyguard for the multi billion dollar big pharma industry. Without legal representation from a top tier group like GP, prepare yourself for even more mishaps.

My comments above are simply my opinion and nothing more.
I'm enthusiastic at times however I am NOT a professional trader.
Please contact a financial consultant for investment advice.