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I'll tell you sometime. Its crazy he even brings it up. Has nothing to do with him. Pm me on x
And its not a sin to tell the truth.
It's only a sin if one doesn't except it.
Or they forgave me. People do that.
RDGL
It is a great board for sure. Best info then whats here. Let me think about it and get back to you Sunday.
Thanks!
My computer shows a picture of the moon at submission, and another picture of Neptune after approval. What does that mean? 😁🥸
Thats my point. Ha!
Some people kids I yell ya.
RDGL
Why did it go up without a new catalyst?
RDGL
Here she comes.....
RDGL
Friday the .13s?
RDGL
LOL, thanks, now everyone knows the secret.
Come on man, i already gave more info then I should of. Suppose to be a secret recipe. Ok ok, crunchy but thats all im giving.
I have a tumeric and peanut butter paste I put together in my garage that I think cures skin cancer. I'll submit for a chunk of Moonshot and let you know if I get it or not.
Moonshot will not grant money to a OTC company. When we get to human trials, and on big board with positive data, I believe Korenko will have better chance at receiving a grant from the Moonshot program. And get this....when we are in second phase of human trials, cancer patients can use the "right to try" program that Trump put in place. Which I think is a great idea. No joke!
RDGL
Great idea.. Send the link to Doc or Twitter media personal.
RDGL
Never say never.
Any money marked for cancer programs or research is not a joke.
RDGL
Moonshot program isn't a joke and its very much still on the table here.
RDGL
Mayo Clinic Training With Radiogel is Complete.
Another step closer.... #MayoClinic #NewGeneration #CancerTreatment #CancerAwareness #Cancer #RadioGel #VivosIncUSA #IsoPet $RDGL pic.twitter.com/tXttdLIHCp
— Vivos Inc. (@VivosIncUSA) April 10, 2024
Yeah i heard the IDE second quarter submission that Doc supposedly been lying about is taking place soon. Or at least what few on here claim won't happen.
Our time has come.
I'll vouch with 100% accuracy your statement is credible. Matter of fact, I also received a similar response. Sorry glo-stick, I'm not into show and tell.
RDGL
Merry Christmas Everyone!!
Safe travels!
And Korenko is worth every cent those shares produce and then some.
Right its not. But if they apply for a IDE and its denied, you wont have to worry about getting wet in a pool, cuz there might not be one.
I have not a clue what Docs plans are. If he has 100% confidence in approval, then sure, let us know when they submit. But we all know how FDA works for small Pharma's.
Doc just did it with BDD. Why not with IDE?
Not worried at all. This ticker is made for longs not day traders. Not sure if Doc will announce IDE submission, but if he does announce, guess who jumps in and rides up to IDE decision then jumps out?
I myself would like to see RDGL trade-up organically on its value per the market strength, and not from a bunch of day traders. So I'm good if Doc surprises us all with a IDE approval PR.
It is 100% true.
How does the FDA Decide Whether to Grant a Breakthrough Device Designation Request?
What is the FDA guidance on breakthrough device designations? The FDA has a rigorous process to ensure the safety and efficacy of medical breakthroughs, including a thorough review of applications of breakthrough technologies. The FDA looks at the scientific data and patient outcomes when submitting an application that weighs potential advantages over existing treatments available to patients. A breakthrough device designation carries with it special priority reviews, intense guidance, and urgency when remediating any issues. Through the Breakthrough Devices Program, the FDA can grant designations for those devices that can offer significant improvement compared to existing treatment options for individuals in need – ensuring each patient receives the best care possible.
FDA breakthrough device designation is granted to novel medical devices that have the potential to provide more effective treatment or diagnosis
What are the Benefits of the FDA Breakthrough Devices Program?
Breakthrough device designation from the FDA can provide a vast array of benefits to medical device companies as well as patients in need. For medical device companies, having your product on the breakthrough device designation list expedites regulatory processes, providing a fast track to FDA interactions and accelerated reviews that bring life-saving devices to market sooner than the standard submission route. The expedited review for breakthrough medical devices results in faster and more efficient development timelines. From a patient’s standpoint, providing treatments and technologies that could help in ways previously felt unreachable can drastically improve the lives of countless individuals
Starting BO bid is $5 billion. Know what you own.
Mods, another great post to be stickied Please.
Radiogel.com
Thank you!
Well done Radiogel investors. Let today's news and future news be a warning to all that the Doc is in full force in getting Radiogel into humans asap.
Delete old post and refresh your browser.
Ok, get back in and when it asks for a post number enter tthis number and hit ok or submit. 168787
If you already have a post up, you need to take old one down first.
The goal of FDA Breakthrough Devices Program is to get potentially life-saving or life-improving innovative medical technologies into the hands of patients and healthcare providers faster.
These are called Sprint Discussions
Sprint discussions are a series of discussions held on a specific topic within the time period set by the sponsor (aka you). These discussions allow for rapid and repeated interactions with FDA about a single topic. Because FDA hopes to engage with breakthrough device designees early and often, the goal of sprint discussions is to reach an agreement in a shorter time frame than would occur by a typical pre-submission process.
MODS!!!! Please sticky this post.
Or take yourself off mod position and let someone else do it.
Congratulations y'all for sticking it out and not listening to the constant bile put out by the 3 stooges. Todays news is bigger then you think. So hold tight.
MERRY CHRISTMAS!!
And #5 is not a IDE issue but a huge bonus if it does work.
Number 4 is all on Mayo Clinic. And I believe it is completed. After FDA green lights Radiogel then Mayo Clinic will be up to speed and ready for first in human treatment.
Vivos lost one of their good one's. Its going be tough to replace his media talent. R.I.P Cam.