When the time comes, you'll be judged for your actions.
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Thought you were done for the day?
You wanna join the DR Korenko onlyfans waiting list?
FACTS
It is generally recommended to create certification training for a new radiology device after successful completion of clinical trials. Here's why:
Benefits of waiting:
Safety and efficacy: Clinical trials ensure the device is safe and effective for its intended use. Training based on established safety and efficacy data provides users with better guidance and minimizes potential risks.
Standardized procedures: Clinical trials typically involve developing standardized protocols and procedures for using the device. These protocols can then be incorporated into the training, ensuring consistency and optimal use.
Data-driven training: Clinical trial data provides valuable insights into the device's performance and potential challenges. This data can be used to develop more comprehensive and targeted training content.
Regulatory compliance: Some regulatory bodies may require specific training for users of medical devices. By waiting until after clinical trials and regulatory approval, the training can ensure compliance with these requirements.
Guess you will be selling up in light of this news?
Great exposure
200000k followers on Facebook..not too bad.
Can't wait for the synics to weigh in
Any idea of the number of cbs17 viewers?
Great - so it's already been shot, just needs a release date?
CBS update?
Do you who's coordinating it?
Funny thing is, the baggy grasshopper doesn't understand how the efs pre submission process works and thinks the FDA hasn't seen the data
24/7. DM and I'll send you my only fans
Ps, don't lose your temper this time
24/7.. Stockholm syndrome
Without ISOPET we wouldn't have the BDD.
Facts are facts
I'll set up an only fans for you soon too sweetheart
24/7.. Stockholm syndrome
Without ISOPET we wouldn't have the BDD.
Facts are facts
Another post that triggered..so funny
Without ISOPET we wouldn't have the BDD.
Facts are facts
Read it and weep grasshopper
Dr. Rebecca A. Krimins is an Assistant Professor in the Johns Hopkins Medicine Department of Radiology and Radiological Science, with additional appointments in the Department of Anesthesiology and Critical Care Medicine and the Department of Molecular and Comparative Pathobiology. A native of Annapolis, Maryland, Dr. Krimins completed her B.A. in biology at the University of Chicago, and received her D.V.M. from Ross University School of Veterinary Medicine. Dr. Krimins completed a one-year small animal rotating internship at the Western College of Veterinary Medicine, University of Saskatchewan, Saskatoon, Saskatchewan, Canada, followed by a one-year surgical internship at Western Veterinary Specialist Centre, Calgary, Alberta, Canada. She worked in private practice as a general practitioner in Hoboken, New Jersey before completing a three-year veterinary anesthesia and analgesia residency at Purdue University School of Veterinary Medicine while also obtaining a MS in Veterinary Clinical Sciences. Dr. Krimins has more than 15 years of experience in managing critically ill patients during advanced imaging procedures and performing ground-breaking clinical studies. Her specialty in veterinary anesthesia, sedation and pain management in combination with her experience in directing advanced clinical research offers each veterinary patient the best opportunities for diagnosis and therapy. As founder and director of the Veterinary Clinical Trials Network at Johns Hopkins University, Dr. Krimins has built a revolutionary center designed to leverage the expertise and platforms available at Johns Hopkins University in order to transform newly discovered diagnostics and therapeutics into real-life practical approaches that benefit veterinary patients. She is editor of the textbook Learning from Disease in Pets, A One Health Model for Discovery, and has been invited to lecture at international conferences.
They are in love with Dr K, I suspect a bad case of Stockholm Syndrome.
they won't need a R/S
plenty of shares to offer once the IDE is approved to fund trials and then stair step from there
Accusing a SEC filing company of a pump and dump..sheez. another receipt.
Keep em coming.
Upcoming monthly/ quarterly update
Upcoming podcast on Twitter (per Twitter investor)
Benzinga hire
Possible CBS news segment Sunday on Moose’s story(per Moose’s owner via Facebook)
Upcoming IDE submission
Probable IDE Approval
Human trials at the MAYO Clinic
Probably lots more that we’ll find out in the quarterly update .
What a great time to be a shareholder in RDGL!
You're always calling for this to go to 4 or 5 cents while claiming you own shares.
Don't be a moron, we don't believe you.
No meeting required to file an IDE
Through Maggie?
You forgot the last hour and last minute of the 1/4.
What happened to your 4c call. Lol
I'd imagine the disgruntled ex-employee would be super sad right now. They missed the boat, in fact ...they nearly sank the boat.
Lucky the Doc could see the deadwood and cleared it out.
Looks like the haters are too embarrassed to show their faces today.
You've got to laugh at the some of the predictions here.
22-mar-24
Hard to see IDE approval in next 9 months (remainder of 2024) given RDGL still can't make Radiogel to FDA standards, Mayo docs remain uncertified, etc. If MK is planning on submitted before all such issues are sorted, best that can be hope for is a conditional approval, aka more FDA meetings before they green light human trials.
Get yourself a calendar Nostradamus
Still too scared to say Vivos lied in a 10-k?
Says a lot about the little pollo's.
Tick tock..24/7