VentriPoint Diagnostics Ltd (VPTDF)

[supervalue]

We’re back to fifty

[supervalue]

Fifty cents week now

[supervalue]

PPS high over 49 cents today !

[supervalue]

Fifty cents soon guaranteed !!

[supervalue]

Fifty cents this week !!!!!!

[supervalue]

Back to forty soon

[supervalue]

Replaces MRI would be doctors buying this stock

[supervalue]

More green fifty cents soon

[supervalue]

Price moving green just slow dollar coming

[imjake]

I am very impressed with what Adams has done with this company. If Covid hadn't hit, this stock might have been close to a dollar by now. Here is a zoom interview/update that is very informative:

Highly recommend watching it! Their machine will be used in the pet industry, mainly dogs, and they're also talking about using it on horses! Dollars coming!!

[imjake]

Well, they are trading again. Not much excitement though. Put in a low bid but didn't get filled. Pretty good volume at 730k.

[imjake]

More News with attachments probably on the website: https://www.ventripoint.com

Dear Friend;

It has been a long time coming but we are back! or almost there as you will read in the attached news release. Here is some background:

1. The Company asked to have its stock halted December 12, 2019 - we were NOT suspended by the Exchange.
2. We received approval to stay halted until we completed the $1,220,000 private placement, which we did last Friday. No one expected it to take so long but COVID-19 disrupted everyone’s plans.
3. The Company actually benefited overall from the pandemic, which you will read about, but briefly we had more access to cardiologist and received a lot of government support (like many other companies). This allowed us to make major changes to almost every aspect of the VMS+3.0 to lower the barrier to adoption, reduce manufacturing costs, accelerate analysis and rewrite the entire source code. The key initiatives attachment is a long read (5 pages), but worth the time.
4. The major advantage of all this work is we no longer have to go to a hospital to install the machine, calibrate the probes and train the staff. It is all done remotely now. You will read about all the advantages this approach has created for us and our customers.
5. The hospitals, while focused on COVID, did continue in their processes to acquire a VMS+3.0 and so we have 11 major hospitals ready to acquire a system as soon as they re-open their echo labs. This is starting to happen as hospitals have to start dealing with regular cardiac patients.
6. We now know COVID wrecks havoc with the heart, especially the right side, and so cardiologists are very interested in our capabilities as they fear the heart problems induced by COVID could go on for decades.
7. Lots more news to come and lots more information on what we have been doing and why it is important on our revamped website and in the addendum..
8. We are in the final stages of the TSXV Exchange review to allow us to resume trading and so I expect that will happen very soon.

I am very thankful for all the people who encouraged me to keep going. It has not been a lot of fun, but we are in a very good place right now - a way ahead of where we were before we restructured. Our team has done remarkable things in the last 9 months and the responses we are seeing from cardiologists are reflecting that we have finally gotten through all the barriers to adoption with a device that is user-friendly and fits perfectly into the workflow of an echocardiography lab. I look forward to telling you all about the wonderful effects doctors with the VMS+3.0 are having on their patients, as well as how well the company is progressing to build value for its shareholders.

As usual, I thank you for your support and interest and if you have any questions or comments, email, text, call.

Regards,

Dr. George Adams ICD.D
Executive-Chairman
Ventripoint Diagnostics Ltd.

[banderas76]

Ok It are 6 mio extra shares as warrants
But it could be much much more

The announcement will tell us a lot

If really good we could go to 0.4
If fluff we stay at 0.05

[imjake]

Yes, I've been on an email list from Adams. There was a PR attached to the email. It is probably at their website. I'm kinda concerned about the convertible debentures that made up this $1.22M offering. Toxic financing?? It's explained in the PR but it is greek to me.

[banderas76]

Did you get that letter of him?
Great
Looking forward to the PR before trading resumes

[imjake]

Here is the email I received just now:

Attached is the news release for today documenting we have closed the second tranche of $495,000 of the private placement to complete the round (which we announced many months ago) with total gross proceeds of $1,220,000.

Here is some background:

1. The Company halted trading and ceased operations in December 2019 to restructure with a new Board and the return of Dr. Adams as acting CEO.
2. The Company closed a first tranche of the $1,220,000 financing February 9 ,2020 with proceeds of $725,000 and resumed operations with all key employees returning to work.
3. In March 2020, COVID-19 pandemic reached Canada and Company ceased manufacturing and fulfillment of orders to hospitals as hospitals were focused on COVID-19 operations.
4. The Company has been focused on eliminating barriers to adoption and enabling remote installation and training.
5. As of Sept 11, 2020 the Company has closed its financing with the remaining $495,000 of proceeds and now has the funds to fulfill its existing and forthcoming purchase orders (more about this in next NR).
6. The Company is in a “Resumption Review” with the TSXV Exchange and expects to be trading in the next few days and will provide a comprehensive corporate update prior to the resumption of trading.

As usual, if you have questions call me.

Regards,

Dr. George Adams ICD.D
Executive-Chairman
Ventripoint Diagnostics Ltd.

[banderas76]

Depending on the opening price it would advise you
To enter as soon as possible after opening... if partnership
With a big one is announced!

[imjake]

Like Adams said, there are shareholders who want to get out, too. I'm curious as to what price the MMs will open trading at. Looks like the last trade was around a penny. I just found this company so I have no shares. Naturally I'd like to see it open as low as possible in order to get a good starter position. I think a partnership with a biggie is one of the announcements coming. Also, maybe an equipment upgrade or improvement. This is very similar to Lexagene, a medical device company, just starting commercialization. Even the price point of $50,000 is the same before discounts.

[banderas76]

Yes indeed

The video is impressive

You noticed following

George Adams expect a wild day (first trading day) like 3 years ago when it went from
0.10 to 0.9

Tony mentionned that several announcements will be made before trading
Will be resumed

What s your guess on news?

News on study on COVID
More sales
Partnership with us / European big company


Sp could go crazy depending on news (0.20-0.50)

I have 400k shares at 0.25 average

[imjake]

This company has turned itself around and is about ready to rock! They've already had installs in several locations. Here is an up-to-date video with Dr. Adams filmed on Sept. 9, 2020. Any day now, maybe Monday, it will start trading again.

[imjake]

Doesn't look good for the company. Here is their last press release: Toronto, Ontario, December 19, 2019 – Ventripoint Diagnostics Ltd. (“Ventripoint” or the “Company”, TSXV:VPT, OTCQB:VPTDF) wishes to clarify the news release of December 17, 2019.
The Company is not in receivership and it has not made an assignment under the Bankruptcy and Insolvency Act. The Company is organizing a private placement and expects to resume normal operations in the new year."

That, of course, was 8 months ago so they may be in bankruptcy by now. The 12/17/19 release describes their funding plan which must not have happened. Getting involved with China is BAD news especially when you have no money to defend your property. I will try to contact Adams and see if there is anything salvageable with this stock.

[teq0904]

Sales pitches are demoed online now.

[teq0904]

Trading might be another month off until the final financing close occurs, but at least the company has started work again.

[teq0904]

Financing is progressing.

[Golden Cross]

VPTDF Tier Change = OTCQB to Grey Market

[teq0904]

"I love trading halts because there is no news yet but I get to read the made up news of feeble minded posts from those who have persecution complex. It is so much fun watching them huddle together dependent on their fellow like-minded simpletons to pool their paranoid imaginations, discussing why they were born under a bad sign and someone has manipulated the sp downwards. etc."
Read more at https://stockhouse.com/companies/bullboard?symbol=v.vpt&postid=30447817#jvmMrTmytCxlClQq.99

[UCParadise]

Halted...another PP???

[teq0904]

This Ventripoint video has never worked and stockdaymedia does not answer phone calls about it
https://stockdaymedia.com/news/radio-interviews/ventripoint-diagnostics-joins-everett-jolly-on-the-stock-day-podcast-vptdf-november-25-2019/

[xwing229]

I was wondering if they’ll keep disclosing each sale or they’ll just put a nr when it’s a huge order. New CEO might change how they disclose them

[teq0904]

Hopefully we get sales in the next week, since they have been to Europe a month ago.

[teq0904]

New video.

Explains why Justin L joined and that the tech integrates well with all devices on the market.

[tedpeele]

Thank you teq0904 for your thoughts on that!

[teq0904]

Dear Friend;

As I wrote yesterday the FDA clearance (their word for approval) could come any day and it came late yesterday. Here is the news release and some background:

1. The US market is one of the largest single markets for medical devices in the world. We estimate that it would take 16,000 VMS+3.0 to deal with all the patients who get echocardiograms per year. This number is growing at 7% per year (1,000 system per year more each year) with an expectation of 25M people over 65 years by 2030.
2. We are now approved to market the VMS+3.0 so we can contact several major centres who have indicated they wanted to know as soon as the VMS+3.0 was clearance for clinical use.
3. The label remains the same that the VMS+3.0 can be used on "any patient where the results are warrants or desired”, which means all the attending doctor only needs is to desire the analysis be done to help with the diagnosis or monitoring.
4. I remind you the VMS+3.0 is a portable device which can be added to any existing 2D ultrasound machine (GE, Phillips, Siemens, Toshiba, Samsung, Mindray…) and be operational in a few minutes. It now allows for patient movement during the exam and has a continuous user guide for the exam as well as the analysis. These features have made it very user friendly.
5. In addition, it is inexpensive to manufacture, which will allow us to offer it as “razor-razor blade” or per use sale to accelerate adoption.
6. FDA clearance helps us worldwide as everyone knows how difficult it is to get FDA approval.
7. This is a major milestone for the company, which has been a long time coming, but has finally arrived. The company is undervalued at $6M market cap. If we were a pharmaceutical company with a FDA-approved orphan drug for a $1B market we would be trading at 10-20 times this market cap. The news today should tell people we are a company with a large market opportunity.

[teq0904]

There is nothing to hold up sales if he gets more marketing companies involved, and lots of studies have been done showing it helps diagnosis for different heart issues so hospitals should have keen interest as more of them purchase it and testify at conferences that it is great.
More studies are planned which will prove its use for other applications too.

[tedpeele]

Hi, thanks for all of the posts. Good news today on approval. Investors in US don't seem to know about this company yet.

I read in an older post that some aspects of the tech will take years for meaningful sales. Just getting into looking at this - may I ask your take on sales growth short term and long term?

[teq0904]

Dear Friend;

Attached is the news release from today. Here is some background:

1. We have installed three VMS+3.0 systems in Western Canada - two in paediatric centres and one in an adult cardiac centre. They are being used clinically on patients, as well as for research to expand its applications. The customers report they are very pleased with the ease of use and analytical results. This is great to hear as we worked very hard to improve the usability of the VMS+3.0.
2. St. Michale's Hospital will be the fourth major cardiac centre to get a VMS+3.0 as it is built passed QC and we can walk it over to them any day now. In addition, the ultrasound technologist there has been helping us with improving the usability and so is fully trained already. They can use it as soon as we can get the IT folks to let us install it. The IT folks at hospitals are always busy and so usually the limiting factor in scheduling an install. We have worked with them before so it should be very soon.
3. We have two more VMS+3.0 systems built and ready to be installed in Eastern Canada - one in a paediatric hospital and one in an adult hospital. We are also expecting an order from another adult cardiac centre.
4. Our sales team was in Europe last week and did many demos. We expect orders from these centres soon, as well.
5. We continue to wait for the FDA response to our submission. Could be any day now.

[teq0904]

It is a September 13 video. At 5:40 he says there are 8M contrast media echo procedures in the US every year, which is a billion$ business in itself. Meanwhile we are starting the 5th month waiting for the FDA eggheads to approve it. Maz hospital is expanding the study to 50 now, but the first 25 were right on point so success is guaranteed.

[teq0904]

FDA drags on, for no reason. This is a minor issue and should have been checked off long ago, but GA said they continue to try to finish it.

[teq0904]

Attached is the press release announcing our manufacturing facility has been certified and is shipping the first VMS+3.0 products to hospitals in western Canada.

Here is some background:

1. We announced back in June that we stop using a contract manufacturer, which we had used for VMS+2.0 and create an internal fabrication facility at our head office in Toronto.
2. This was possible as the VMS+3.0 is a much simpler and less-costly machine to fabricate due to the new tracking method which is a simple circuit board embedded in the adaptor for the ultrasound probe.
3. Of course we had to have the facility certified before we could begin to manufacture devices and this was achieved Thursday last week.
4. We have now fabricated the first two VMS+3.0 in this certified facility and will ship them tomorrow or Friday to fulfil the first two purchase orders, which were from a Heart Institute and a Children’s hospital in western Canada (their policies are not to allow third parties to name them in press releases).
5. This is major milestone for the company and its mission to improve cardiac care for children and adults.
6. It has been an amazing summer so far with Health Canada and European approvals for the VMS+3.0, the establishment of the new manufacturing centre and now first sales - all in under two months.
7. We have more orders coming soon from Canada and Europe will come back from vacation in September and again a number of sites have indicated they are ready to purchase the new system.
8. We are still awaiting US-FDA clearance and have been told the agency is working to complete their review as soon as possible. Again we have hospitals ready to acquire the VMS+3.0 as soon as it is approved in the USA.
9. Our Chinese partners are also advancing their sales pipeline and expect to have first sales very soon.

[teq0904]

It has already taken longer for the FDA review these minor changes than when we got a major label change from one chamber to all 4.

[teq0904]

Still waiting for the ivory tower FDA to make this simple approval.

[teq0904]

Update on HC approval. Mazankowski Hospital study due any day now, and we know that it is going to be positive since they presented at the VPT booth on the weekend.

Attached is a news release announcing the Health Canada approval for the next-generation VMS+3.0. Here is some background:

1. We started to develop the VMS+3.0 18 months ago as soon as the VMS+ was approved based upon the upgrades doctors, sonographers and patients requested.
2. The first step was to invent a completely new tracking system, which we have now filed a patent on and allows for patient movement during the scanning and collection of 2D images. Even though the exam is only 2-3 minuets, patients still found it difficult to remain motionless. Sonographers were also challenged in getting some of the views without repositioning the patient. This is a major upgrade to the usability the system.
3. We also included a step-by-step guide into the exam procedure to allow sonographers to be sure they acquired all the necessary views. This guide also has the recommended location for the anatomical landmarks for the analysis of the views and so again the doctor knows exactly what is required in each view.
4. As we reported earlier, the human factors study showed 100% of clinicians were able to be quickly trained and remembered how to use this new guided process. This will greatly improve the consistency of the results, which up until now were so variable that doctors do not even look back at the previous echocardiogram. They have told us many times, it would be great to be able to compare exams over time.
5. From business perspective, the VMS+3.0 is much cheaper and easier to manufacture. As announced we will be assembling it in house and therefore have cancelled the contract manufacturers for the VMS+.
6. More importantly, the VMS+3.0 is much smaller and so is portable. Our sale people can take it with them on all sales calls, set it up in minutes and allow potential customers to use it at their sites immediately. We will be doing these in Canada starting next week now that we have approval.
7. We also have hospitals and cardiac clinics in Canada waiting to submit the paperwork to acquire the VMS+3.0 and we have already notified them we can now supply the VMS+3.0 immediately. We will be announcing these installations as they happen.
8. Overall, the VMS+3.0 is smaller, easier to use, allows patient movement and promotes consistency. This is the tool everyone has been asking for and we look forward to demonstrating it to cardiac centres in Canada.

[teq0904]

Dear Friend;

Attached is a news release, which announces our successful Human Factors Study with operators to verify the user-friendly and easy-of-use of the VMS+3.0. Here is some background:

1. Recently, we announced the filing with Health Canada, Europe and US-FDA for approves to market the VMS+3.0. All agencies have accepted our submissions as complete and they are under substantive technical review at this time.
2. As a new part of all medical device submissions is a “Human Factors Study” to verify that the software can be easily operated and understood by users. We conducted a study with clinicians wherein we trained them on the VMS+3.0 and then sent them away. A few days later they returned and were tested to see if they could operate the VMS+3.0 without assistance. We were overjoyed to have 100% success. Everyone easily was able to operate the system.
3. This study proves the the system is easily learned and not easily forgotten. The study participants even commented on how intuitive the system was and how it was obvious to them even in the training how to use the VMS+3.0.
4. The “ease-of-use” part is one feature of the upgraded system along with the guided procedure and no more need to keep the patient motionless. These are the features users of the VMS+2.0 had requested.
5. From a business perspective, the VMS+3.0 is much cheaper and easier to manufacture. As a result, we have established manufacturing for the VMS+3.0 in our headquarters. The lower mill cost will have a significant impact on our margins. The device is much smaller and is now portable. This makes it possible for our sales people to take it with them and do an on-site evaluation. These on-site evaluations are also what potential customers have been asking for. They want to be able to scan a patient and reconstruct a heart before committing to initiate the process to purchase the VMS+3.0
6. We are looking forward to exhibiting at the American Society of Echocardiography next week in Portland, Oregon. This is the largest conference of the year which is dedicated solely to cardiac ultrasound. The Mazankowski Heart Institute has a presentation on the VMS+ at the conference and will be reporting on their study of the reduction or elimination of contrast media in technically-challenging patients, which have “unreadable” conventional 2D echocardiograms. We believe the VMS+ can “read” the “unreadable” studies and there will be no need for contrast media. We await the report of their independent clinical assessment.

[teq0904]

I am expecting a few $ from this stock. I have 293k shares and 1,105k warrants.

[teq0904]

Today's email Attached is a News Release announcing we have filed in Canada, Europe and USA for approval of the VMS+3.0. Here is some background:

1. These applications document the VMS+3.0, with the new tracking system and updated software, is equivalent to the VMS+. We are not asking for a change in label so from a regulatory standpoint these are relatively minor changes. From a user standpoint the changes, which allow for patient movement, easier placement of the VMS+3.0 within the echo suite and guided exams and analysis, are major advancements.
2. The last time we submitted to these agencies for approval for the VMS+, we received Heath Canada approval in a week, CE mark in 2 weeks and FDA in 6 weeks. That application was a change in labelling (from RV-only to whole heart analysis and some hardware changes). While it is not always possible to predict the behaviour of these agencies, we are hopeful a similar timeline will be achieved.
3. We have also completed a human factors study wherein sonographers were trained on the VMS+3.0 for 3 hours and then tested the next day to to see if they could operate the system correctly. All 13 passed with 100% and commented how intuitively obvious it was to operate the VMS+3.0. More on this in a later news release.
4. Our sales people have been chomping at the bit to get out and sell the VMS+3.0 and have lined up a number of demonstrations, as the new system is portable and can be set up in a few minutes. On-site evaluations are now possible anywhere in the world. We have major sites waiting for the VMS+3.0 to be approved so they can immediately evaluate it and conduct clinical studies to show its value in patient care and cost reductions.
5. With the MAJOR conference of the year the American Society of Echocardiography (ASE) coming up on 3 weeks, this is excellent timing to launch the VMS+3.0, which we demonstrated the prototype at Euroecho and a few regional conferences events already. This will be its first exhibition at an international event specific to ultrasound analysis of the heart.
6. At the ASE, the Edmonton Heart Centre will be presenting the results of their study of the ability of the VMS+ to analyze “unreadable” echo exams of the left ventricle (LV) and avoid the need for injection of contrast media to obtain a result. This will spotlight the VMS+ and its cost reduction potential at the conference. More on this in a later news release.

[teq0904]

Approval applications were sent today per the nr. We will have all 3 approvals very shortly per the last email from GA.
It appears the 20 year wait for sales is over, because the only thing holding back sales was the difficult operation of the ancient tracking system. Cost is down with the new one and it is patented so this will be the cardiac diagnosis system that everyone moves toward from expensive and time consuming MRI.

[teq0904]

Dear Friend; Attached is a news release. Here is some background:
1. The VMS+ with analysis of all 4 chambers of the heart using 2D or 3D ultrasound was approved a year ago by the US-FDA. Ongoing consultation with the cardiology community identified ways to improve the VMS+ to make it more user-friendly as well as to reduce the cost of production. The result was the development of the VMS+3.0.

2. A key novel component was the creation and patenting of a tracking system based on modern microcircuits and advanced positioning software. This new tracking system was also established to allow patient movement during the exam, which was a major source of error and the most common complaint from sonographers, who usually move the patient to get the best window for scanning. Since the Company now manufactures the new tracking system, the cost is a fraction of the off-the-shelf system we purchased from an outside vendor and used in all previous VMS versions.

3. The Company has completed a usability study with 13 cardiac sonographers and they unanimously found the VMS+3.0 intuitively easy to learn and use. More on this in a future news release.

4. The next step is to complete the submissions to the US-FDA, Health Canada and Europe. These are minor submissions as we are not asking for a change in the label, simply updating them on the change in technology and sending them the data to show equivalency.

5. We anticipate the approvals will take a few weeks and so the sales team are gearing up to close some sales based on the delivery of the VMS+3.0. This is good timing as the MAJOR conference of the year is the Annual Congress of the American Society of Echocardiography and this year it is in Portland, June 21-25. While it is unlikely we would have US-FDA clearance for the ASE, we will likely have Canada and Europe and the congress is attended by cardiologists from all over the world.

6. The new tracking system will make it much easier to integrate the VMS+3.0 into an existing 2D ultrasound device and we are assessing various devices to see which device and company would be the best partner. Again more on this later.

I know it has been a long haul, but making cardiac diagnosis and treatment better for all and especially for children is worth it. I believe the new VMS+3.0 is the clinical tool cardiologists have been waiting for.

[teq0904]

http://thecbq.ca/ventripoint-diagnostics-tsxv-vpt-ceo-george-adams-diagnosing-heart-disease-faster-safer-and-more-affordably/

[teq0904]

The update today says they are finessing the motion sensors so FDA can't happen before that is complete. It is patented though, so will be worth the wait.

[teq0904]

FDA application will be in the next week.
Taken from the MD&A.

Meeting with MD Anderson pg. 17

"The Company announced on June 4, 2018, only a few weeks after obtaining FDA clearance, thatMD Anderson Hospital had ordered a 4C-VMS+ to use for routine clinical assessment of oncology patients to determine cardiac changes during and after treatments. The machine is operational, and the staff trained. It has been used on a number of patients and the Company is meeting with the principal cardiologist in May, 2019 to assess their experience to date. MD Anderson has been one of the top two cancer centers in the USA for decades."

Maz in May - Page 18, end of first paragraph.

The reduction in the number of contrast-enhanced 2D echo studies would represent a significant savings in time and costs for echocardiology departments. It would also reduce the need to inject the patient with contrast media. The use of contrast-enhanced ultrasound is increasing in the western world with the burgeoning population of heavier peoplemaking it more difficult to obtain clear images using ultrasound.On July 17, 2018, the Company announced the study had begun and the research team reports a publication will be coming out in May.

VMS 3.0 Technical Glitch/Delayed Q2/Q3 - Top of page 29.

During 2018 the Company beganramping up sales and marketing efforts, however, with the announcement of the next generation VMS+3.0 System in development(see NR August 8, 2018), which eliminates the need for patients to remain motionless during image acquisition,improves the workflow of the VMS+ through a more intuitive user interface, and has a much smaller footprintwith an innovative new tracking sensor technology, many potential purchasers opted to wait for the launch of the new system once regulatory approval is received. Aside from two sales of the current VMS+2.0 systems in early 2019, expected sales ramp up has been delayed until after regulatory approval has been received.

Given the average 12-18 month sales cycle to hospitals, we do not expect to see revenues from the VMS+ 3.0 to be recognized for accounting purposes until Q4 2019 (i.e. after delivery and clinical acceptance).

The Company had expected to be able to submit the 3.0 for approval in Q4 of 2018, however, a technical issue with the new technology, now resolved, held up the submissions to Health Canada, European CE Mark and the FDA. Applications for approval are expected to be submitted in early May, 2019.