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Please read the November 20,2020 PR again then read January 19, 2021 PR again. these two PRs give me more reason to believe we are in a good position now that the EFS IDE has been submitted. I can only hope that the delay in submission from end 2Q to end 3Qish was to dot i’s and cross t’s.
I just looking at charts and seeing some common occurrences. No other merit to it besides me wanting this to start stair stepping up. Been here 4years and am patient but would like some clarification on timeline from company
Let’s tap 0.0978 then bounce to .15
Crazy how volume is 150k one day and the next nearly 2million. I’m anxiously waiting for the three weeks of 20-30 million volume stretch
Pps went down but only from $12k worth of shares I’m not worried at all
It’s staying in this channel until significant update on timeline is more predictable
Ok everyone what’s fowardly?
Should be getting update on the recent isopet treatment of Jackie. It’s been a few weeks. Should have seen a response already if it trends the same as all of the other procedures in the past
Lots of early volume. I wonder if something is coming and this is the shake and bake before the bounce. Tomorrow is Friday and it’s possible we are into the latter half of the potential 30 day window of acceptance/approval of IDE
Shake and bounce coming
Not sure why the page is being switched up.
Great post
Agreed. Did the same
If you build it they will come my friend. It is being built now.
Proven technology
Approved in animals
In talks with fda
Mayo Clinic
IDE in work
Yeah I guess he could have more but if he sold all of them he’d be a millionaire right now. Yet all he does is accumulate more which means something positive to me
It takes me a long 40 hour work week for a tiny check. I have my shares and will have the patience needed. Been in this stock 4 years and have witnessed the stepping stones taken to get to where we are. I can work as many more 40 hour work weeks needed knowing this stock will have its day. I’m long and strong here. If you looking for a quick flip this is not for you. If you are looking to have your face hurt from smiling from ear to ear when that day comes then stay
I just want to know when the fda accepts the application and when a decision on approval will be to move forward into our next phase
Correct me if I’m wrong but the doc converted 150,000 warrants for 0.045 for approximately $7,500. Then sold those shares (58,000) at .115 for approximately $7,000.
But the FDA changed their approach timeline given it was taking them so long and companies were going out of country to pursue improvements on their innovations. Hence FDA timelines have shrunken to …see page 20 -21 https://mdic.org/wp-content/uploads/2018/12/MDIC-EFS-Blueprint-for-EFS-Success-2016.pdf
So we are years out?
To include the fact that the initial ide submit talk was delayed and using the days between initial target submission until now could have been steps 1.2.3
I hope I am, but this is my opinion I thank you for your opinion as well but collective group talk helps everyone
I also appreciate your input as at least you have something to say that requires thought and research versus others on this board. In short I personally think IMO that the press release should read that rdgl submitted a presubmission ide versus submitted ide. That’s the clarity needed and everything else we say or think is google based and deductive reasoning as to ensuring we as investors know what is the most accurate and up to date information on rdgl
You don’t submit an IDE until after the presubmission meetings were discussed. Therefore when the first line of the press release says they submitted the ide it means they already had the presubmission meeting hence the term “presubmission”
-Rdgl - contacts FDA about efs ide
-Rdgl has presubmission meetings
-FDA gives rdgl direct support of what they need rdgl to do
-Rdgl does it and submits ide
-Now they both rdgl and fda stay in contact throughout the process
If you read the PR from September 20th it clearly states they submitted the IDE. They submitted based on the press mission meetings with the FDA which means they were already on step 2 and 3 of the previous article I posted. Not only that but the IDE was submitted with Mayo Clinic’s clinical trial protocol which is under review simultaneously as the IDE.
Also interesting information on page 26.
“In the IDE submission, the study should be clearly identified as an EFS. Since the EFS is a small study (limited number of patients and sites), it does not require registration on www.ClinicalTrials.gov.”
https://mdic.org/wp-content/uploads/2018/12/MDIC-EFS-Blueprint-for-EFS-Success-2016.pdf
This is what I found. See table 2 on page 22 -25.
My thought is we are on step 4. Now 10 days into the roughly 30 day review cycle
Also note the approvals table above that and the awesome shortening of the review also and approval process
You just make up your own stuff don’t you.
Patience. Not sure why some are freaking out a little. Look at the last 4 or 5 news releases and or tweets. Reread them over an over again and ask yourself again why are you in this stock. I’d love a fda ide timeline just like the next person but the reality is that we still submitted the ide and still wait on fda acceptance and then hopefully approval. I also wanted to see a spike in stock price but I’m not so mad that I’m getting out of the stock but rather still accumulating my shares of the fortune.
Dummy boy is ready and I’ve been ready for awhile now!
I’m joking people lighten up.
What are you talking about lol
Two 911’s showing up, I don’t know what else they have to say at the moment
X a bunch more lol
Well that’s .90 - 1.50
Anyone want to provide a collective recap on all recent news and post/tag it for the top
Agreed
Can’t say I agree with this. Potential is there but I’ll just sit back and wait. Plus I only want longs joining the party
8 tweets my bad
Agree but damn 5 tweets and 2 news releases in 3 days needs to be spread out a little lol.