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Well done Gramps. I have posted a summary of your letter couple of weeks back. The most important thing is the reply or correction. I didn't see both
So simple all of us should email or call Andy or Paul.
Guys, longs. All these days your positive posts when company is trying for bigger things were promising and boost to other shareholders. But the most important trait I saw is that when company isn't making good decisions you chose to question and express concern. Hats off. We need change.
More than FDA decision, CVS and other PR's, more worrying is the longs revolution(particularly Simpsonly , DewBoom, Steve etc). I have expressed my vent in an email to Andy. Yes we need to start a campaign to stop a wrong person sitting in a wrong chair.
Nice to see you back Simpsonly. Feels great to have you here on the board. I wish I can contact you outside this board. Do you have an email or other means? Thanks brother, nice to see our positive and practical guy back.
Just that someone doesn't find actipatch in each of 9800 stores is not all a problem, as we have actipatch in only around 300 stores to start with. And our longs doing great job with photo proofs. Can't help bashing and you know why. Seems like it's going right direction and by the intensity of bashing, something is coming up and very soon.
What is the Timeline for new application fot FDA clearance? ETA
Couple of steps back for a lion doesn't mean it is losing and accepting defeat, it really means it is ready to pounce and attack with full might and force. Go Biel
Ohh , you should be from India and AP
Another rtply from Andy "We are not leaving the FDA behind. Sree is on vacation this week. Next week we will file a notification for a new 510(k) using the same data and just excluding the men. The VA, Mundipharama, hospices sale, UK etc. are all moving ahead"
Email reply from Andy "Thank you for your support. The FDA took a myopic view of the data. We had an adverse group of men with low initial pain scores that distorted the data. We are going to simply refile the 510(k) with the just the women’s data and get clearance for musculoskeletal pain in women. "
Get a spokesperson, get the CVS going, get the VA deal reachable to all VA hospitals, try advertising, get the international sales up seriously, let the people and sales put FDA to shame.
Could be. Never late than never. I seriously doubt that FDA will announce BIEL is accepted in the challenge.
Wait, your words still don't sell. Form is temporary, but class is permanent. It's a temporary choke but we will get back better.
Slipper shot to FDA. When all countries and institutions like NHS, B Braun, Mundi etc believe this product, why not FDA unless they are sold out.
So, what's your take as how company will take further action and steps. I know we GG&G will not sell as the product only drives us.
We may be denied today but we are not selling, you know why, the product works. Don't get surprised if the same FDA announce Biel as challenge winner and take credit.
Why wouldn't BIEL mention FDA approved device on the CVS inventory?
How I wish Actipatch cures psychic's when used on head.
I went by Indian way of using commas. But the value is same. Maybe misleading for some
Hahhahaha $166,000 fine settlement with SEC. you can clearly understand who is at wrong end. So SEC wants to get out with something rather than losing and dragging it. It may be late but truth prevails. SEC is one thing that was stopping some newbies according to previous posts. One by one slipper shot replies for all those false claims.
And what makes you think it's not worth? Until couple of years back it was a fight with FDA trying to make them understand what it is and create a class for themselves. Why would all big names like NHS, B Braun, Dr Scholl's, Boots, Llyods, clinical trials from big universities, CVS have belief in this product? One thing I can tell "No one knows before a miracle happens , and no one need to be told after miracle happens". The se is the case with BIEL. It is a miraculous product- it needs mass attention by advertising which company cannot afford now but soon. Why all those positive reviews by the users, if a tech is giving satisfaction to 10% of the users it is still a very good tech but BIEL is working for 60% of users. Couple of years back FDA approved a cancer drug which will work only for 1% of lung cancer patients. This is my last post. We are tired of explaining. Do your DD. Lots of posts here is an encyclopaedia of info.
And you know what most of the longs here been for a decade and we know what it is worth, we are not new to these turbulences. And going by the history we are very near.
You know what, I better not read the posts until FDA approval, which is imminent. Can't see impatient investors who are feeling bad due to some deadlines given by posters as if FDA is giving those deadlines. Unnecessary projections week after week giving bad effect on the stock.
You should expect a PR before the market bells ring. And it will be released through all major PR channels. That is what they usually do
Longs doesn't easily let their shares loose as they know and believe in the company since a decade. The frenzy selling is by the newbies who unnecessarily trapped in deadlines war created by a few.
All panic caused by the unnecessary naming of FDA approval deadlines without substantial evidence. And people are going frenzy leaving BIEL. I will wait until FDA decides.
Useless deadlines for FDA approval given on this board and unnecessary hype. FDA will happen when it should happen and on schedule within the FDA limits.
Well it depends on how you see the product. All reputed institutions gives a green signal and we still call it snake oil. It also depends on the agenda to spill negativity for accquiring more shares.
Patience !!. Scare tactics going on. Same games again and again. MM's game. Used to these games since a long time just before news
Wow lot of Newbies here, Hmm something fishy. Hold on longs, fishing rods with baits are ready to demoralise you for your shares
Your answer about Keith. BIEL added Keith last week on their website management portfolio as part of their website updation.
Long and accumulating since then. Not sold single share
Guess you should be from India, particularly AP. Long here since 2010
My take on FDA: Who knows, FDA is wantedly delaying the current application. If Actipatch is approved then in less than a couple of weeks there will be a huge buzz and all over news. FDA could be thinking that they want to take the credit and create buzz for these revolutionary products through their program, hence delay?
The efficacy of any product in this world is not 100% and same with BIEL's. If you are in the percentage of the product not working for you, no worries you can move on and that doesn't mean it doesn't work for the 70+% of the users.
Watch out for BIEL. Can explode at any time. Do your DD.
Wow..New investors on the board. Do you smell something folks? News?