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gimmee greenbacks

05/04/19 9:32 AM

#179593 RE: pennytiger #179586

Completely agree pt, it's the FDA's role to ensure products are safe and effective. PERIOD. Actipatch and it's technology has already been cleared as safe and effective by the FDA. The only issue at hand is the degree of effectiveness which is an unreasonable and unethical standard not evenly applied to every other product or medical device imo.

Daytime_Lantern

05/04/19 3:10 PM

#179622 RE: pennytiger #179586

Yes, I agree! Curve balls are being thrown around all over the place by BIEL and the FDA. This stuff needs looking into by an entity with investigative talent. But in the meantime, we shareholders should challenge BIEL's management in whatever way possible. Of course, as shareholders, we are in a weak position to make a serious impact on corporate behavior, as per our current situation. But please, let us not wait around like sheep and be financially slaughtered by these, to be generous, incompetents, but at worst, tricksters, mountebanks, etc. This fiasco is happening in real-time, right in front of us, so there is no excuse for sitting idly by and not do something. I propose a plenum group to be formed, through this board. This group will be the vanguard for shareholder issues, and concerns. We must organize folks! It will be totally transparent, for its activities will be conducted via board access and interaction. If this proposal is prohibited by board policy, than we should get this under way off line. Do I have any volunteers? Something has to be done, and done now, or we will lose it all without a fight. Our clarion call should be... We Fight! We Fight! We Fight!

GLTA!!!

2Relax

05/06/19 8:36 AM

#179728 RE: pennytiger #179586

Penny, IMO we would already have approval if Andy could just stay the course with the dream team. But he thought he learned enough after gaining two approvals with their help in 2/17.

Again, Andy seems to jump the shark every time.

The main reason I think they should have stayed with the dream team is becuse I expect the approval process to become even more difficult now that the FDA knows that he's navigating thru this difficult terrain alone (the FDA can use any excuse because Andy has NO BACK UP), FDA is about to be knee deep in the fight to keep big pharma on top.

They expect this fight because they see how close HEMP/CANNABIS is to becoming recreationally legal, ending the prohibition (people will self medicate because their are less side effects from
H/C). Now dozens of electricueticals about to hit their desk for approvals, things are about to change bigtime for big pharma. Don't worry, the FDA will be right their to prop them up when they get blindsided.

I look at the FDA as the blanky for big pharma. If only Andy had better skills at navigating thru this, obviously he doesn't.