At the start of December 2020, Flemish newspaper De Standaard included a special look at innovation in the region.
As part of the campaign, DSP Valley spoke with Media Planet about the importance of networking to digital innovation. CEO Dieter Therssen explained DSP Valley’s philosophy and the benefits networking brings.
“Innovation is never the work of a single company, but often arises from a combination of existing data or products. That implies that you need several companies to realize innovative developments. A good network is one of the key factors for successful innovation.”
At DSP Valley, we work toward business development in a collaborative spirit, leveraging networks to benefit entire markets and ecosystems. As Dieter put it, “Our biggest challenge is the translation of the technology to the industry. DSP Valley tries to play a role in this. Several things are needed: you need technology, you need people with the talent to convert that technology, you need money, but you also need a network to bring companies together around good ideas.”
DSP member Verhaert Masters in Innovation has received a research grant from VLAIO to develop state-of-the-art artificial intelligence (AI-)driven robot technology.
In the research project, Verhaert will develop a robotic platform for spinal surgery which uses algorithms developed by Deep Learning (AI). The developed algorithms will transform high resolution preoperative 3D images, like CT scans and MRIs, to high resolution images of the patient in his or her new physical laying position during surgery. The novel part of the proposed procedure is the significant reduction of the use of cancerogenous ionizing x-ray beams during surgery, like CT-scans, while still being able to perform sub-millimeter surgery and catheter tracking.
3-step surgical procedure Defining the concept The physical laying position of the patient changes before, at the start and during surgery, which has an impact on the physical position and form of the spinal cord. All these changes in position need to be taken into account in order to perform sub-mm surgery.
Before: the patient is laying on her back for high resolution CT/MRI scans.
At the start: the patient is laying on her stomach.
During: the patient is laying on her stomach and slightly moves because of breathing, heartbeat and the impact of the surgery itself.
A high resolution sub millimeter 3D image is taken from the patient several days before surgery. This is done either by a CT-scan or MRI. Typically, the scan is taken while the patient is laying on his/her back. Based on the image the surgery is planned and a trajectory is calculated in order to reach the desired location in the spinal cord.
At the start of surgery At this stage the patient will be laying on his/her stomach. Markers are placed on the patient which are detected by a set of Infra-Red cameras in order to create a 3D model of the patients’ physical position on the operating table. In this new position, a low dose low resolution (supra-millimeter) 2D image is take of the patients’ spine. The 2D image is taken with a C-arm 2D fluoroscopic scanner.
The 2D image and the external marker localizations are used to transform the high resolution pre-surgery 3D image into a newly reconstructed high resolution 3D image of the spine in its new position and form. At this point, the surgeon and its team has a 3D image of the patients’ anatomy in combination with an external reference frame.
In the Netherlands, 300 to 400 people are infected per year with the legionella bacteria (Legionnaires’ disease or Pontiac fever), a number that is rising each year. Victims of the bacteria suffer for a long period, from several months up to more than a year. Between 5 and 10% of cases are lethal.
Legionella infections mostly occur through people breathing in legionella-contaminated aerosols. Aerosols are small droplets of water that are generated, for example, when showering. For this reason, public showers like the ones in sports centres, swimming halls, and saunas, as well as truck stops and camp sites, need to be flushed regularly to prevent legionella growing in the water pipes. The required flushing is often done manually or semi-automated, which is very time consuming, prone to human errors, and labor intensive. Especially when one takes into account the legal obligations to report data like date, time, water temperature, and flush duration per shower.
The risk of legionella contamination has increased in the current Covid-19 crisis with the (temporary) closure of facilities. Showers are not used by clients and facility engineers who have to stay home and are not allowed to come to their facilities for the requisite flushing.
Sfella is the Smart Flush solution by Mioto* that addresses all of the above issues. Sfella is a user-friendly, reliable and easy-to-install solution for legionella prevention. The system is modular, for use within environments with multiple showers. It assures flushing the shower(s) happens after an operator-defined time period. The system reports the important flush data like date, time, duration, and water temperature. This reporting and control of the showers happens locally or remote via a dedicated gateway.
Sfella is powered by the mesh network MyriaNed. It is an infrastructure of nodes that connect directly, dynamically, and non-hierarchically. This allows easy configuration and scalability. Data transfer to and from the shower units (represented by a node) is wireless and bi-directional. Therefore, settings can be changed remotely, while the report with flush-related data can be received remotely in your email inbox. MyriaNed can be configured to use either 868MHz or 2.4GHz. This allows for the optimal fit in each local environment in terms of coverage and energy usage.
In February 2020, just before the first Covid-19 wave struck the Netherlands, van Mierlo Ingenieursbureau B.V. started a pilot program with Sfella on 15 showers in a care institute. The unforeseen Covid-19 crisis forced the care institute to close its sports facilities for several months, a perfect period to test the installed Sfella system. It appears the automatic flushing happened every 72 hours as programmed. Once the facilities opened again in early summer, final confirmation arrived: examinations of the water samples taken showed no legionella contamination in the related water pipes. This offered the most convincing evidence that Sfella delivered.
van Mierlo Ingenieursbureau is now to actively approaching the Dutch market and discussing with sales and distribution partners, as well as technology partners, to broaden the Sfella roadmap. If you are interested in partnering for sales and distribution, including outside the Netherlands, please contact us.
CellSine is a revolutionary new technology for early stage drug testing. It could easily mean medications brought to patients faster and with less testing on animals. A win-win!
The technology behind CellSine, based on electrochemical impedance spectroscopy (EIS), was developed as part of a doctoral research project at the University of Leuven (KU Leuven) and the University of Brussels (VUB), resulting in a proof of concept. As anyone who’s brought a concept to market knows, though, this is but a step in a much longer process.
That’s where Comate came in. As they put it themselves, “CellSine relied on the expertise of Comate’s engineers and designers for the technical development, to translate the PoC into a market-ready product.”
Thanks to Comate’s expertise in taking a proof of concept to market, CellSine has launched a truly innovative device. Their ambitions run high, including integrating AI to their data analysis and boosting personalized medicine.
DSP Valley active in Flexible Electronics and Healthcare
Healthcare is a major market for both established and emerging technologies. Flexible Electronics is a growing field gaining more and more momentum. Flexible electronics in healthcare is a combination with a bright future.
As our Newsletter readers and members will know, DSP Valley is currently active in three Flexible (and Wearable) Electronics projects: Flexlines (focused on creating a one-stop-shop for flexible electronics), SmartX (specifically geared towards flexible electronics in textiles), and SmartEEs (aimed at helping innovative companies digitize). This is by design: flexible (and wearable) electronics have high potential. This is in part because of their many possible applications.
One of DSP Valley’s core programs in Smart Health. We’re co-founders of the IBN flanders.health. This year, we’ve worked hard alongside our partners Flanders.bio and MedTech Flanders in getting a Spearhead Cluster for Health Tech off the ground in Flanders.
Collaborative Digital Business Breeding
Our work in the health technology and flexible electronics sectors is essential to our central mission: breeding digital business through collaborative business development. The European Flexible and Wearable Electronics projects and the flanders.health IBN and coming Spearhead Cluster are concrete examples of creating collaborative business opportunities. These go beyond single company, or even single application, vision and seek to build and support strong ecosystems that will be economically sustainable.
This is why we were delighted to read IDTechEx’s analysis. The abstract of their report “Flexible Electronics in Healthcare 2020-2030” confirms DSP Valley’s perceptions. It reinforces our resolve to continue to work hard to bring Flexible Electronics and Health Tech together, in our region and beyond.
Click here to read the summary sent to us by IDTechEx. Please note that we have nothing to do with their research. This is neither an endorsement nor a promotion.
Join us to find out more
Want to find out more about our Flexible (and Wearable) Electronics projects? Check out the upcoming FREE events – click the titles for more information and to register:
Flexible Electronics WebinarFlexlines unites different players providing access to new Flexible Electronics technologies through one-stop-shop concepts in order to accelerate the design, development, and uptake of advanced applications in Flexible & Wearable Electronics.
SmartEEs information Session with TNOThe SmartEEs Project is funded by Horizon 2020 and is aimed at supporting SMEs and Mid-caps in integrating flexible and wearable electronics into novel (series of) products.
In this webinar, Corne Rentrop (TNO) and Dieter Therssen (DSP Valley) will explain all about the project and what the benefits are for companies and service providers thinking about applying.
SmartEEs Information Session with imecThe SmartEEs Project is funded by Horizon 2020 and is aimed at supporting SMEs and Mid-caps in integrating flexible and wearable electronics into novel (series of) products.
In this webinar, Dieter Therssen (DSP Valley), Maarten Cauwe (imec), and Frederick Bossuyt (imec) will explain all about the project and what the benefits are for companies and service providers thinking about applying.
IDTechEx sent this report summary to DSP Valley. You can read more about DSP Valley’s activities regarding Flexible Electronics and Smart Healthcare here.
NB: We are sharing this summary as a service to our readers and members. We are in no way affiliated with IDTechEx.
IDTechEx Report Summary
“The market size for flexible electronics in healthcare will exceed $8.3 billion by 2030”
Dr Nadia Tsao, Principal Analyst at IDTechEx, recently published the below article on the topic of flexible electronics within the healthcare industry.
Flexible Electronics in Wearable Cardiac Monitoring Technologies
In today’s digital age, focus on digital health and the quantified self have led to the rapid rise of heart rate monitoring technologies through wearables such as fitness trackers and smartwatches. Such devices have already proven their ability in detecting hidden heart conditions such as tachycardia and atrial fibrillation in seemingly healthy people. However, the majority of wrist-based devices currently serve only as an advance warning, they are not approved by the FDA for use as medical devices. Thus, cardiologists still need to use alternative technologies for their diagnostic and monitoring needs.
This is where flexible electronics comes in. Cardiac monitoring requires devices to make close contact with the skin, making devices that integrate flexible and even stretchable electronics ideal due to their ability to conform to the skin, the potential for a low profile, and overall patient comfort. IDTechEx forecasts that flexible electronics in cardiac monitoring, deployed in electronic skin patches and electronic textiles, will be a $2 billion market in the year 2030.
IDTechEx have been reporting on flexible electronics for the past decade and have recently published “Flexible Electronics in Healthcare 2020-2030”. In this article, IDTechEx describe how electronic skin patches and electronic textiles are used in cardiac monitoring. To find out more about other technologies for monitoring cardiovascular health, please refer to the IDTechEx report, “Cardiovascular Disease 2020-2030: Trends, Technologies & Outlook“.
Electronic Skin Patches
Electronic skin patches are wearable devices that contain electrical components which are attached to the skin, typically using an adhesive.
In cardiac monitoring, electronic skin patches present an interesting balance between the medical standard, which is a 12-lead ECG test, and consumer electronics such as smartwatches and fitness trackers. While electronic skin patches offer less data than can be obtained through a 12-lead ECG, they present more useful and accurate information than the optical technology used in smartwatches and fitness trackers, and offer continuous monitoring, unlike the 1-lead ECG in the newer smartwatch models.
Within medical applications, electronic skin patches bring increased mobility to the patient over the 12-lead test. The first step from the 12-lead ECG is the Holter monitor, a portable, wired, device designed to be used over 24 – 48 hours. However, this device remains unwieldy and intrusive.
To increase patient comfort, companies have developed cardiac monitoring patches in the form of 1 integrated device over a flexible substrate. By removing the wires and decreasing device footprint and weight, electronic skin patches are more comfortable to wear, and can be used for longer monitoring periods, up to 30 days. This longevity is critical in detecting events for patients who do not experience them daily. The next step for devices will be to incorporate printed electronics to manufacture integrated electrodes and devices with even close-fitting designs for greater patient comfort.
Overall, electronic skin patches for cardiac monitoring fill the gap between in-patient cardiac monitoring (accurate, safe, non-ambulatory, expensive), implantable cardiac monitors (accurate, less safe, ambulatory, expensive) and other wearable fitness devices (poor accuracy/no medical approval, safe, ambulatory, cheap). But the deployment of cardiac monitoring skin patches is not just limited to event monitoring or mobile cardiac telemetry. Outside of cardiac monitoring, electronic skin patches for monitoring of other diseases (e.g. respiratory), or general patient monitoring (in-patient, post-discharge, etc.) also contain cardiac monitoring capabilities.
Electronic textiles, or e-textiles for short, are products that involve both electronic and textile components in a single device. The idea is to combine the functionality from electronic components with the comfort, esthetics and ubiquity of textile products.
Smart clothing for sports used to be the major focus in the e-textiles industry – companies have made many attempts to develop mass-market products. Though e-textile companies may choose different strategies and technologies, the end products all have very similar functionalities such as tracking of activity, heart rate, respiratory rate, etc. There remains sporadic interest from apparel giants for sports applications, but many of the e-textile players have now shifted towards healthcare applications.
There is a close match between sports and medicine as the same vital signs are being detected and the same form factor (clothing) can be used. Within smart clothing, companies can design in 12- or even 15 leads for ECG readings, much more than the 2 – 3 offered by electronic skin patches. Moreover, smart clothing can be much more comfortable than electronic skin patches. The latter often causes discomfort through issues such as skin irritation. Despite the higher regulatory hurdle in healthcare vs sports, companies see the long-term benefit of e-textiles in healthcare. Smart clothing that is as comfortable as everyday clothing while still delivering medical-grade data will be key to automatic and continuous monitoring of patients going about their daily lives.
E-textiles are not just limited to clothing as a form factor, they may be incorporated into non-apparel textiles such as bed sheets, blankets, and even furniture. Regardless, the key for e-textile players today is validate their product through regulatory bodies such as the FDA, and to look into reimbursement for their products.
The COVID-19 pandemic has forced clinicians around the world to test out medical technologies to continue treating and monitoring their patients remotely. Though many physicians will eventually return to in-person practice, a fraction will continue utilizing telemedicine and remote patient monitoring technologies. Technologies such as electronic skin patches and e-textiles have much to offer to the healthcare system – remote patient monitoring has been shown to result in better outcomes, higher quality of care, and increased patient satisfaction. Healthcare systems will achieve cost savings through better management of patients and thus avoiding costly hospitalization and emergency room visits. While reimbursement of remote patient monitoring technologies is moving in the right direction, it will remain a major hurdle for companies entering this space.
Dr Nadia Tsao is a Principal Analyst at IDTechEx where she has been driving the company’s research in the life sciences. Her research spans a range of topics within healthcare, including digital health, bioelectronic medicine, and tissue engineering.
At DSP Valley, we love to see our member organizations succeed. We’re happy for them, of course! We’re also thrilled to see our digitization ecosystem thriving and rewarding innovation. That’s why we’re delighted to share exciting news about one of our startup members, Helpilepsy.
Managing Epilepsy with Digital Technology and Personalized Medicine
Launched in 2017, Helpilepsy is a platform for both patients and their care team to monitor epileptic seizures, side effects, medication and other parameters. Billed as “a complete digital solution for people with epilepsy and neurologists,” the software allows for more personalized approaches to Epilepsy in patients. Currently, patients and doctors in 5 countries (Belgium, Luxembourg, France, Germany, and Hungary) use Helpilepsy, with more expansion on the horizon.
It works like any app: a patient can download it on their app platform of choice (the Apple store, Google Play, etc) and begin using it. Physicians and healthcare workers can track and monitor patient inputs through beautifully visualized web dashboards.
This summer, the team announced an exciting development: official ISO13485:2016 certification, with many thanks to their Quality and Regulatory Lead Amandine Berton. This may not sound like a huge deal, but it’s a big achievement, especially for a small startup team.
ISO certification pertains to a manufacturer’s quality management system, which in turn involves their documentation and processes. All new releases need to be fully documented, the team must be able to show clinical proof of their software’s effectiveness, new employees must go through a welcome checklist, and more. These must comply with ISO13485 in order to meet European regulations. EU regulations govern myriad elements, including customer feedback, logistics, development and more — all before a product can be sold with the CE mark within the EU single market.
The CE symbol, which we probably all recognize but never really think about, indicates “that products sold in the EEA have been assessed to meet high safety, health, and environmental protection requirements. When you buy a new phone, a teddy bear, or a TV within the EEA, you can find the CE mark on them. CE marking also supports fair competition by holding all companies accountable to the same rules.”1 Crucially, it is up to manufacturers to make sure their products adhere to CE standards and EU regulations.
Recently, the rules regarding medical devices and medical technology changed. From now on, medical software including apps like Helpilepsy and the team’s newest product, Migraine Manager, fall into a higher classification. This means that they are subject to much stricter oversight. Affected class I medical software companies have been given until 2024 to fully conform to the new regulations.
The fact that the Helpilepsy team has been able to secure ISO certification ahead of the deadline is a testament to their talent and dedication.
While ISO certification, and subsequent CE marking, is administratively necessary, it brings with it tangible benefits. For one thing, the team is ahead of the game. The biggest part of their work to fully comply with new regulations is complete. They can once again focus on their core business!
Moreover, the processes necessary for the certification lend further credibility to Helpilepsy’s technology. It’s a strong selling point that they can offer to potential patients, doctors, and business partners.
What’s more, as co-founder Ludovic Ampe explains, ISO certification will hopefully be a catalyst for further expansion. Since the CE mark is a European-widely recognized standard, achieving it should open up more international markets.
Innovating in the field of medical devices can get extremely complicated and overwhelm even the most experienced engineers.
For startups all the necessary areas of expertise can prove be too much, but even for well-established medical companies it is not an easy task to keep up with the ever-changing field, increased complexity and regulations of medical devices.
Areas of expertise
The first thing you need is a multidisciplinary team that covers all the different areas of expertise. For startups, this is often impossible, and they need to look for external services to complement their skills. If you take this external route, look for teams that are flexible and can work well together with your team. Look for a team that has an extensive history in medical products and other fields. They can provide a wealth of expertise and experience in various areas that even some medical device manufacturers may lack internally. This will ensure you look at your project from different angles and transfer solutions from other fields.
Experienced design firms have tried and tested development methodologies that will guide you through the whole process. They know where the pitfalls are, and can work according to the required ISO standards.
Start from the user
Human factors, user-centric design, and usability engineering play an increasingly important role in the medical device industry.
Designing for healthcare must start from the user (patient, doctor, caregiver), not the technology. Particularly crucial is designing for human factors from patient acceptance, to increasing patient and user safety, to minimizing the risks of potential human errors.
Acquiring insights into user needs, fears, and use from patients and workers is essential for designing a successful medical device. Therefore, extensive user research and testing are an absolute must in the development process.
Medical devices are not stand alone anymore. Many products are connected to platforms and exchange data with patients, doctors, and caregivers. This requires new insights and disciplines to design frustration-free user interfaces, secure data protection, and interconnected products.
Additionally, some healthcare is shifting away from hospitals and other medical environments to patients’ homes. Connected smart products collect medical data and make it available for patients, and doctors, in real time, to make the right decisions. This not only makes the development of products more complex, with smart censors and high connectivity, but also demands a complete rethinking of how healthcare services are delivered. These products become product-service systems that require a service design expertise to make them successful on the market.
Finally, when you have your minimal viable product, proof of concept, and final prototype, you must be able to produce it in a consistent error-free way.
Thinking about this is not something you start with after the design is finished. Design for manufacturing should already be part of the design process from the very beginning. Production and product cost need to be taken into account at the very start of development.
Finding the right partner to produce your product is also essential, and if you start early enough, a good partner will help you in the last stage to go to production.
Go to market
Established healthcare companies have the necessary expertise to market their products in-house. For startups this can be a challenge. Even the best designed product can fail if it is not brought to market the right way. At the start of the development, product marketing and branding must already be part of the thinking process. This is the only way to make sure they will reinforce each other and avoid unpleasant surprises at launch.
How does Achilles face medical design?
At Achilles, we advance healthcare through people-centereddesign. We prototype early and often, to ensure we keep the people we design for at the heart of the process. By putting ideas in the hands of users from low-fidelity paper interfaces to 3D-printed prototypes and high-level immersion VR, we systematically identify improvements and preventively exclude risks without compromising our intuition.
We believe better health is achieved by engaging people at every stage of their health journey. Our cross functional team — consisting of biomedical engineers, designers, usability experts, and a doctor — work across disciplines to integrate people’s needs with responsible technology and sustainable business models. We strive to establish innovative healthcare service solutions that drive business value by advancing the standard of healthcare.
Visit Achilles Design at MEDICA Düsseldorf from 16-19/11/2020.
In July, Citylab fully integrated its work for the Innovative Business Network (IBN) Smart Cities Vlaanderen with partner DSP Valley. “After more than a year and a half of successful collaboration with DSP Valley, it is time for this step,” says Citylab director Marc Schepers. “By bringing our business cluster fully under one roof, we will become more effective and create room for further development of Smart Cities Vlaanderen!”
DSP Valley and Citylab are the driving forces behind the IBN Smart Cities Vlaanderen, which was started more than a year and a half ago with the support of various big names in the tech world. Although still at an early stage as an organization, the cluster has had a promising start, successfully bridging the gap between business and government. Their strength has been converting Smart Cities issues into concrete business cases for companies.
The two organizations are convinced that they are coming together at the right moment. Schepers declared, “It is now time to connect even more and to continue our cooperation with DSP Valley. That is why we decided to fully shift our co- promotorship to DSP Valley.”
From his perspective as CEO of DSP Valley, Dieter Therssen emphasizes the need for an encompassing structure. “In Flanders, several initiatives have emerged in the field of smart cities in recent years , but there is not yet an overarching approach across the region. At the same time, the demand from local governments for smart city solutions is increasing exponentially,” he states.
CEO of Living Tomorrow and president of Smart Cities Vlaanderen, Joachim De Vos agrees that the time for joining forces is ripe as the movement for smart cities gains momentum. This merger between DSP Valley and City Labs is the first step toward an even stronger Smart Cities Vlaanderen consortium.
Flanders Innovation and Entrepreneurship (VLAIO), which financially supports the consortium through its subsidies for IBNs, is also on board. Asked for comment, a spokesperson confirmed, “This evolution makes the position of Smart Cities Vlaanderen more powerful and stable and allows them to support companies even better in the smart cities domain. It will enable the cluster to actively contribute to developing Flanders into a smart region.”
The integration between Citylab and DSP Valley “enables us to accelerate our role as a matchmaker between companies and local authorities, building business consortia and creating a digital platform in the quadruple helix,” says Peter Vandeurzen, Cluster Manager for Smart Cities Vlaanderen. DSP Valley will further expand and strengthen the cluster from its office at the Corda Campus in Hasselt.
A bundled structure can also be the starting point for jumping from Flanders to Europe in the context of digitization. By coordinating smart cities initiatives, the desired critical mass and strength can be achieved to make Flanders a leading smart region in Europe.
All information about the Smart Cities Vlaanderen community and how to participate can be found on their website.
Smart Cities VlaanderenCluster The cluster was founded by a number of steering group members and co-financed by VLAIO. The founding steering committee members are: Living Tomorrow with Joachim De Vos, chairman of the steering group, Nokia, Cronos Group, MyCsN, Tractebel Engie, Mediahuis, Hydroscan, Niko, and AllThingsTalk.
Together for strong, ambitious innovation More starters, more stayers, more growers: that’s what we aim for! The Innovation & Entrepreneurship Agency and the Innovative Business Networks want to facilitate cooperation between companies, knowledge institutions and governments. Smart Cities Vlaanderen is one of these innovative business networks. Discover the others at the website. #growingstrong #sterkgroeien
To help face COVID-19 and ensure both health and well-being, the European service provider in product innovation Verhaert Masters in Innovation developed ‘Hai’: a digital demonstrator platform, based on user-centered Artificial Intelligence.
New platform Hai for safer behavior
After 3 months of lockdown, strong regulations, and economic struggle, we’re carefully going back to our “normal” life. It’s a challenge to find the right balance between the well-being and health of the population, and a steady recovery after this critical period.
To provide an answer to this challenging situation, Verhaert developed a demonstrator of a digital platform that uses AI-based Computer Vision to extract essential metrics from any room or area. The ‘Hai’ platform can bring COVID-related safety awareness to the public, allowing them to make informed decisions. It’s not a surveillance system, but a tool to empower people with relevant data about a specific space and to nudge them in a positive way towards a safer behavior.
Components of the AI system
The digital platform consists of 3 components:
Cameras to record a live feed of the people present in a particular area, the people entering and leaving the place.
An edge AI system to process the footage on-the-fly. The system extracts the number of people, how many of them wear face masks, and measures the physical distance between individuals.
Online dashboard to display this information in a friendly and educational way.
Let’s say you work at your desk and you want to get something from the cafeteria. On the dashboard, you can see whether or not you should wait a while until fewer people are present at that place.
Artificial Intelligence algorithms
Verhaert’s AILab trained the AI algorithms to calculate the number of people present in any space and detect how many of them are wearing face masks. What about the security and protection of private data? The cameras’ live feed never leaves the AI system. The edge AI device treats the information locally and only transfers processed and anonymous data to the dashboard. No human being sees, stores or transfers any images, safeguarding everyone’s identity and privacy.
Hai is about our health
The online platform is a tool to organize ourselves and our spaces, it doesn’t judge individuals. It allows us to access real-time information from anywhere to make informed consent whether or not to enter a room. Hai will display the total number of people in an area versus the maximum quantity allowed. Additionally, it creates a heat map of “close-encounters” (distance less than 1.5 meters) giving valuable information for cleaning, disinfecting, optimizing walking flows, and detecting bottlenecks.
Hai is about you
Hai will recognize in the near future your gestures, so if you wave hello to the camera or raise a thumb, Hai will respond interactively. The digital platform has been created to demonstrate how AI technology can help us in managing our presence and common spaces better during COVID. Ensuring we all stay safe, not only at home.
– – – – – –
Since 1969, Verhaert Masters in Innovation has pioneered the field of product innovation. As a leading innovation group in integrated product development, Verhaert assists companies and entrepreneurs in the development and implementation of successful innovation processes. The group now has more than 200 employees with offices in Kruibeke, Gentbrugge, Kortrijk, Nivelles, Noordwijk, Utrecht and Aveiro.