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Medical Taiwan 2026

MEDITECH Takes Expanse to the Next Level for Nurses and Therapists, Announces Expanse Patient Care

MEDITECH Takes Expanse to the Next Level for Nurses and Therapists, Announces Expanse Patient Care

MEDITECH has disrupted the EHR market with its revolutionary physician mobility tools, and now the company is doing it again for nurses and therapists with Expanse Patient Care. The intuitive, web-based software empowers nurses and therapists to mobilize care delivery using the device best suited for the task at hand, while keeping their focus on what matters most โ€” their patients.

Designed using MEDITECHโ€™s strong framework and understanding of how nurses and therapists really practice, Expanse Patient Care enhances mobility and streamlines nursing and therapy workflows. Use of familiar, mobile devices allows nurses and therapists to โ€œstay on the goโ€ and maintain face-to-face time with their patients. With a smartphone, caregivers can untether from WOWs and conveniently perform bedside verification, review clinical decision support tools, conduct patient assessments, and review the patient record in the palm of their hands.

Additionally, the solution allows for personalized navigation so users can review patient records in a way that works best for them, with customizable features and a user interface similar to their everyday mobile devices. Users can also conveniently review the full patient journey through a single EHR available on a single mobile device, allowing them to collaborate with physicians using a consistent toolset and efficiently navigate care transitions.

โ€œNurses and therapists are the largest user group within the MEDITECH community, so it was important for MEDITECH to enhance our EHR in a way that improves their unique and demanding experiences,โ€ said Cathy Turner, BSN, MBA, RN-BC, associate vice president, MEDITECH. โ€œWe are excited to provide a modern solution that functions on a mobile device to help transform the way nurses and therapists with busy schedules deliver care.

It is well documented that personal and positive interactions between patients and their care teams improve patient satisfaction. By breaking down technology barriers that too often come between nurses and their patients, Expanse Patient Care helps get nurses back to doing what they enjoy most, while also enhancing the patient experience. With Expanse Patient Care, MEDITECH is reducing the learning curve for nurses and therapists and improving their productivity, resulting in higher overall satisfaction for both caregivers and their patients.

China Buys Danish Robots to Fight Coronavirus

China Buys Danish Robots to Fight Coronavirus

Self-driving Danish disinfection robots are now shipping to a number of hospitals in China to help fight the coronavirus, also called COVID-19. This happened after Sunay Healthcare Supply signed an agreement with the Danish company UVD Robots. The first robots shipped this week and in the following weeks, many more robots will be shipped via air to be deployed in the fight against the coronavirus. With ultraviolet light, the Danish robot can disinfect and kill viruses and bacteria autonomously, effectively limiting the spread of coronaviruses without exposing hospital staff to the risk of infection.

Through Sunay Healthcare Supplyโ€™s partners in China, the robots will be deployed in all Chinese provinces. โ€œWith this agreement, more than 2,000 hospitals will now have the opportunity to ensure effective disinfection, protecting both their patients and staff,โ€ says Su Yan, CEO of Sunay Healthcare Supply, a medical equipment supplier to the Chinese market.

Now sold in more than 40 countries, UVD Robots is already delivering its self-driving disinfection robots to hospitals in other parts of Asia in addition to healthcare markets in Europe and the United States. The invention increases the safety of both staff, patients and their relatives by reducing the risk of contact with bacteria, viruses and other harmful microorganisms. The concentrated UV-C light emitted by the robots as they drive has a germicidal effect that removes virtually all airborne viruses and bacteria on the surfaces of a room. Results, that led to the UVD robot winning the robotics industryโ€™s โ€œOscarโ€ โ€“ IERA Award in 2019.

Technology found superior in the market
Before entering into the agreement with UVD Robots, Sunay Healthcare Supply did its due diligence and screened the market for the best technologies to fight the coronavirus.

โ€œWe found the UVD robot to be superior compared to other technologies and are pleased to โ€“ in a very short amount of time โ€“ enter into a reseller agreement with exclusive rights to supply the UVD robots in China,โ€ says Su Yan, emphasizing how both parties have worked intensively to get deliveries of robots to the Chinese hospitals.

CEO of UVD Robots, Per Juul Nielsen, is pleased to be helping combat the spread of the virus in China through the companyโ€™s solution: โ€œIn a severe crisis like this where the world health is threatened, our innovative technology really proves its worth,โ€ he says.

Developed by large group of collaborators from hospital and robotics industries
UVD Robots is a portfolio company in Blue Ocean Robotics, which develops a wide range of service robots.

The development of the UVD robot started in 2014, when a group of Danish hospitals demanded a far more effective way of reducing infection rates in hospitals. The fruitful collaboration between bacteriologists, virologists and hospital staff from hospitals, and robot developers, designers, engineers, investors and business people from Blue Ocean Robotics led to an early market introduction in 2018.

Claus Risager, CEO of Blue Ocean Robotics and Chairman of the Board of UVD Robots, calls it a
tremendous satisfaction for employees, management and the circle of owners to witness the deployment of the UVD Robot. โ€œWe are now helping solve one of the biggest problems of our time, preventing the spread of bacteria and viruses with a robot that saves lives in hospitals every day.โ€

About UVD Robots
UVD Robots is a Danish company established in Odense, Denmark, following a successful co-development project between Odense University Hospital and Blue Ocean Robotics resulting in the unique UV-Disinfection Robot. The UVD Robots provide efficient and automated disinfection solutions for hospitals and life science customers. Application of UVD Robots in hospitals patient and operating rooms save patientsโ€™ lives by reducing Hospital Acquired Infections (HAIโ€™s) and operational costs for hospitals. The UVD Robot has been clinically tested and verified at Odense University Hospital and by independent microbiological laboratories.

About Blue Ocean Robotics: Award-winning Robot Venture Factory

Blue Ocean Robotics develops, produces and sells professional service robots primarily in healthcare, hospitality, construction and agriculture. The portfolio of robots includes brands like; Beam Robots, a mobile telepresence robot for communication, social inclusion and CO2 reductions; UVD Robots, a mobile robot for disinfection; PTR Robots, a mobile robot for safe patient handling and rehabilitation; and a handful of other service robots. Blue Ocean Robotics develops the robots from problem, idea and design to development, commercialization, and all the way to exit. Each robot is moved into its own subsidiary- venture company, making Blue Ocean Robotics the worldโ€™s first Robot Venture Factory.

 

LumiThera to Expand Research into Diabetic Retinopathy for Valeda Light Delivery System

LumiThera to Expand Research into Diabetic Retinopathy for Valeda Light Delivery System

LumiThera Inc., a commercial stage medical device company delivering photobiomodulation (PBM) treatment for ocular disorders and diseases, announced it has initiated further studies with the University of Wisconsin-Milwaukee to establish the use of their Photobiomodulation platform in Diabetic Retinopathy (DR).

โ€œRecent research in our labs in both preclinical and clinical areas have indicated potential in treating diabetic edema with PBM,โ€ stated Janis Eells, Ph.D., Professor, University of Wisconsin-Milwaukee. โ€œOur work shows that early PBM benefits in reducing the detrimental effects of high glucose on retinal cells and early human data is now starting to show benefits in the clinical setting.โ€

DR is the leading cause of blindness in the world. The International Diabetes Foundation 2019 Fact Sheet estimated that globally 463 million people have diabetes now, and future estimates suggest that this number will increase to 578 million by the year 2030.

โ€œWe have been working with Dr. Eells and the University of Wisconsin-Milwaukee on our dry AMD research and the work in DR and Diabetic Macular Edema (DME) is a logical extension of our PBM platform,โ€ stated Clark E. Tedford, Ph.D., President and CEO of LumiThera, Inc. โ€œThe results from Dr. Eellโ€™s lab point to the multiple cellular benefits of treating the disease early and PBM would be an alternative approach for treatment of early disease.โ€

LumiThera was granted a CE mark to commercialize the Valeda System in European Union for the treatment of ocular diseases including dry AMD. The company previously announced that the National Institutes of Health and division of the National Eye Institute have provided a $2.5M grant to support the LIGHTSITE II multi-center clinical trial to lead to U.S. approval for dry AMD. The Company is enrolling two multi-center trials, one in European Union and one in the US for dry AMD. The entry into DME provides a second major ocular disease platform for the Valeda system.

โ€œWe are excited to be involved in the development of Valeda for both non-neovascular (dry) AMD and DME. We are currently enrolling patients in the LIGHTSITE III study and believe that PBM could be an even bigger platform for DME,โ€ remarked Quan Dong Nguyen, M.D., M.Sc. and Diana V. Do, M.D., Professors of Ophthalmology at the Byers Eye Institute, Stanford University. โ€œDME is the leading cause of functional vision loss among working adults worldwide. Treatments with intravitreal injections of pharmacologic agents are effective but can be costly and invasive. PBM could provide a significant improvement to the current practices with its non-invasive approach.โ€

โ€œI am continually impressed with the scientific foundation that LumiThera is building for PBM with collaborations in both preclinical and clinical research,โ€ stated David Boyer, M.D., Retina-Vitreous Associates Medical Group. โ€œThe benefits for PBM on multiple critical cellular pathways involved in the disease etiology in preclinical work is now being evaluated in the clinical setting and could change the way we address chronic disease that leads to blindness.โ€

About LumiThera Inc.
LumiThera is a commercial-stage medical device company focused on treating people affected by ocular disorders and diseases including dry AMD, a leading cause of blindness in adults over 65 and DR, the leading cause of blindness in the world. The company is a leader in the use of PBM for treatment of acute and chronic ocular diseases and disorders. The company is developing the office-based Valeda Light Delivery System to be used by eye care specialists for medical treatment.

The Valeda Light Delivery System has been granted authorization to use the CE Mark by an EU Notified Body as required for commercial use in the European Economic Area only. Valeda is not approved for use by the Food & Drug Administration (FDA) in the USA.

Abbott to Integrate Next-Generation Glucose Sensing and Automated Insulin Delivery Technologies for Seamless Diabetes Care

Instrument-free Molecular Diagnostic Tests

Abbott and Insulet Corporation , the global leader in tubeless insulin pump technology with its Omnipodยฎ Insulin Management System (Omnipod System), announced they are partnering to integrate Abbott’s world-leading1 glucose sensing technology with Insulet’s next-generation tubeless system, the Omnipod Horizonโ„ข Automated Insulin Delivery (AID) System (Omnipod Horizon System), to offer personalized automated insulin delivery and care for people living with diabetes.

Controlled through an app on a user’s personal smartphone device โ€“ a unique feature that will be offered with the Omnipod Horizon System โ€“ the integrated platform will consist of the trusted tubeless insulin delivery Pod and Abbott’s next-generation FreeStyle Libre sensor. Through a simple, intuitive design, glucose data from the sensor will be sent directly to the Pod that is embedded with an algorithm to automatically adjust insulin delivery โ€“ without the need for an additional device, connection or tubing. This integrated system will be designed to always remain in automated insulin delivery mode and can be controlled through an app on a user’s personal smartphone to manually take a dose of fast-acting insulin, or bolus, before meals for optimal performance. Additionally, the integrated platform is expected to be the first combined system with a fully disposable wearable sensor and pump.

Abbott is focused on creating future-forward health technologies that simplify how people living with diabetes manage their condition so they can live their best lives,” said Jared Watkin, senior vice president, Diabetes Care, Abbott. “As diabetes care becomes more interoperable, we’re developing more connected approaches to improve care. Through this partnership, Abbott and Insulet will offer an integrated digital health platform that is simple and accurate and will provide a best-in-class user experience.

“We are excited to expand our partnership with Abbott by building on our consumer-centric Omnipod Horizon platform, which offers unparalleled simplicity, accuracy, and now sensor choice for consumers,” said Shacey Petrovic, President and Chief Executive Officer, Insulet. “As interoperability becomes increasingly important, our approach to automated insulin delivery will change the future of blood glucose management by offering consumers greater choice in algorithms, sensors and overall experience. This collaboration furthers our shared vision to help our consumers put diabetes in the background, so they have more freedom to enjoy life.”

This connected care solution will integrate both the Omnipod Horizon System and FreeStyle Libre sensor data, offering a seamless option that will fit easily into the lives of people with diabetes. With both Insulet’s and Abbott’s ability to sell its products through the pharmacy, users of the integrated platform will benefit from ease of obtaining supplies with an innovative pay-as-you-go model.

ABBOTT’S AND INSULET’S NEXT-GENERATION TECHNOLOGIES
The FreeStyle Libre 2 system, Abbott’s next-generation continuous glucose monitoring (CGM) technology, is currently approved in Europe2 and offers enhanced accuracy and optional glucose alarms at no additional cost from the first-generation FreeStyle Libre system. The FreeStyle Libre 2 system can continuously stream up-to-the-minute glucose data to digitally connected devices. When used as a standalone system, users scan the sensor worn on the back of the upper arm for 14 days to see real-time glucose levels every minute, historical trends and patterns, and arrows showing where glucose levels are going without having to fingerstick.

Expanding upon the current Omnipod DASH Insulin Management System, Insulet has developed and is currently in clinical trials for its Omnipod Horizonโ„ข AID System. The intended design of the technology is to leverage glucose values from a CGM to predict future glucose values and adjust insulin delivery. The Horizon System will leverage the technology of the DASH Insulin Management System on a user’s personal smartphone.

About the Omnipod DASH System:
Insulet’s Omnipod DASH System was designed to serve as the foundation for the company’s future innovation. Designed with patient discretion and convenience in mind, the Omnipod DASH is a continuous insulin delivery system consisting of two simple components: a tubeless, waterproof*, Bluetoothยฎ wireless technology Pod (pump) that holds up to 200 units of U-100 insulin** and a modern, color touch-screen Personal Diabetes Manager (PDM) that controls the Pod. The Omnipod DASH System has a suite of optional mobile apps for users, caregivers and healthcare practitioners to help simplify diabetes management. The Omnipod DASH System, which received U.S. Food and Drug Administration clearance in June 2018, is the only DTSec and ISO 27001 certified insulin pump for cyber and information security and safety.

About Insulet Corporation:
Insulet Corporationย  , headquartered in Massachusetts, is an innovative medical device company dedicated to making the lives of people with diabetes and other conditions easier through the use of its Omnipod product platform. The Omnipod Insulin Management System provides a unique alternative to traditional insulin delivery methods. With its simple, wearable design, the disposable Pod provides up to three days of non-stop insulin delivery, without the need to see or handle a needle. Insulet also leverages the unique design of its Pod, by tailoring its Omnipod technology platform for the delivery of non-insulin subcutaneous drugs across other therapeutic areas.

ยฉ 2020 Insulet Corporation. Omnipod, DASH and Horizon are trademarks or registered trademarks of Insulet Corporation. All rights reserved.

About the FreeStyle Libre System:
Abbott’s FreeStyle Libre technology, the #1 sensor-based glucose monitoring system used worldwide,1 reads glucose levels through a sensor that can be worn on the back of the upper arm for up to 14 days, eliminating the need for fingersticks.3 The FreeStyle Libre portfolio has changed the lives of more than two million people across 46 countries5 and has secured partial or full reimbursement in 36 countries, including France, Ireland, Japan, the United Kingdom, and the U.S. For the U.S.

About Abbott:
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 107,000 colleagues serve people in more than 160 countries.

Flowonix Receives FDA Approval to Market Prometra II Pump for use with Intrathecal Baclofen

Flowonix Receives FDA Approval to Market Prometra II Pump for use with Intrathecal Baclofen

Flowonix introduced the Prometra II 40mL pump to the US market in November 2019, providing patients and clinicians a choice between 20 mL and 40 mL capacities when choosing an intrathecal pump delivery device. The new indication expands significantly the market for the Prometra device by enabling its use in the treatment of spasticity. Flowonix will begin marketing the device with the new indication immediately.

“Over the last several years, physicians utilizing implantable pumps to deliver long-term baclofen infusions have only had one device option,” said Charles Argoff, M.D., a neurologist at Albany Medical Center in Albany, New York. “The availability of a totally new pump to assist in the management of severe spasticity allows for a meaningful new option for those patients who suffer from this condition.”

Unlike the existing motor-driven pump, the Prometra II Pump utilizes a pressure-driven, valve-gated delivery mechanism to deliver boluses of medication into the intrathecal space. This innovative delivery mechanism provides broad spinal cord coverage rapidly and enables novel programming modes of intermittent flow followed by periods of no flow, unique to the Prometra device. The Prometra device also features a 10+ year battery life, which can significantly reduce the number of future surgical procedures patients will need to replace expiring pumps.

The American Association of Neurological Surgeons estimates that spasticity affects more than 12 million people worldwide, with common conditions such as cerebral palsy (CP), multiple sclerosis (MS), traumatic brain injury (TBI), spinal cord injury (SCI) and stroke comprising the majority of that population. While intrathecal baclofen is reserved for the most severe cases of spasticity, the number of patients who could benefit from the therapy is significant.

“This is a major milestone for Flowonix,” said Larry Heaton, President and CEO, Flowonix Medical, Inc. “We believe the community of clinicians treating severe spasticity with intrathecal baclofen will find the Prometra System to be a welcome addition to their armamentarium for treating their patients, and we will be working with leading physicians in the field to establish Prometra as the standard of care in intrathecal baclofen therapy.”

The Prometra Pump was approved for use in the United States in 2012 with an indication for use to deliver INFUMORPH. To date, the Prometra System has been implanted in more than 8,000 patients worldwide, including use of the device to treat patients with severe spasticity outside the United States since its approval in the United Kingdom and European Union in 2011.

About the Prometraยฎ II Programmable Infusion System

The Prometra Programmable Infusion Pump System is indicated for intrathecal infusion of drug therapy, including: Infumorphยฎ (preservative free morphine sulfate sterile solution), preservative-free sterile 0.9% saline solution (Sodium Chloride Injection, USP), and baclofen (baclofen injection, intrathecal, 500-2000 mcg/mL).

About Flowonix

Flowonix Medical Inc. (www.flowonix.com), headquartered in Mt. Olive, New Jersey, is working with healthcare professionals to help improve patients’ lives through targeted drug delivery innovation and therapy advancements. Founded in 2005, Flowonix is working closely with physicians and patients to enhance the capabilities of implantable drug delivery systems. Our goal is to become the leading implantable drug delivery company in the world.

Lucid Diagnostics Partners with Fred Hutchinson Cancer Research Center to Evaluate BE Progression Biomarkers Using EsoCheck

Lucid Diagnostics Partners with Fred Hutchinson Cancer Research Center to Evaluate BE Progression Biomarkers Using EsoCheck

Oman oil and gas exploration and production company, Petroleum Development Oman (PDO) has reportedly signed a contract with the Oman Engineering Procurement & Construction (OmEPC) to boost engineering in the country.

According to the Sultanate’s state-run news agency, Oman News Agency, the contract outlines a joint partnership between the four Omani SMEs that form OmPEC; Value Engineering Centre (VEC), Hamad Engineering Services (HES), Precision Engineering Consultancy (PEC) and Rock International.

The contract for Phase 1, which is valued at $25.9m (RO10m), was signed at PDOโ€™s Knowledge World centre in Muscat by the companyโ€™s managing director, Raoul Restucci and chairman of OmEPC, Mohammed Al Said, representing the four-company partnership.

The Engineering, Procurement and Construction (EPC) contract is structured in three phases.

Phase 1 of the contract spans over three years and covers engineering services. Upon successful delivery, it will then be expanded to cover both engineering and procurement for a further three years; construction management will be added at the end of the sixth year.

The latest development in the oil and gas industryโ€™s In-Country Value (ICV) strategy, the contract is indicative of PDO’s support of Oman’s ICV initiative.

In addition, it is also indicative of PDO’s support of efforts in job creation and training as well as providing commercial and investment opportunities for local businesses, the report stated.

The Sultanate’s ICV blueprint strategy was launched in December 2013.

PDO defines ICV as ‘the total spend retained in country that benefits business development, contributes to human capability development and stimulates productivity in Omanโ€™s economy.’

Commenting on the contract, Restucci said: โ€œThis is an important EPC contract for PDO as it will provide services for our business in key areas, utilising a skilled Omani workforce and providing opportunities for emerging local businesses in supporting their development.”

โ€œIt is a further example of our long-term contribution and commitment to ICV in the Sultanate, creating jobs for Omani people by localising the supply chain,โ€ he added.

Speaking about the joint partnership, Al Said, said: “OmEPC is a result of continuous ICV efforts by PDO to create meaningful employment for Omanis. With this contract, PDO has granted OmEPC an opening not only for employment of Omanis, but also development and growth of local EPC capabilities and capacity beyond the boundaries of PDOโ€™s operations.”

MedForce Announces Preliminary Speaker Lineup and Agenda

MedForce Announces Preliminary Speaker Lineup and Agenda

The organizers of MedForce the Sales and Marketing Strategy Conference for MedTech Commercial Leaders announced the preliminary agenda and speakers for 2020.

The 2020 agenda encapsulates the current issues and future challenges that are front of mind for pharma companies, key topics include:

  • Transform your commercial models
  • Drive customer-centricity
  • Increase salesforce effectiveness
  • Adopt digital marketing
  • Create value added services

Be inspired and learn from 50+ Commercial Excellence, Sales and Marketing leaders sharing practical insights on how to drive performance, boost market growth and achieve greater ROI. Some of the speakers that have confirmed to attend the 2020 edition of the event are:

Rodamni Peppa, VP Business Strategy and Commercial Excellence, Boston Scientific

  • Robert van Geffen, Global Head of B2B Digital & Activation, Philips Healthcare
  • Moritz Fischer, VP Marketing Hospital, Fresenius Medical Care
  • Christian Popp, Director of Training and Development, MITG, EMEA, Medtronic
  • Andrea Miotto, Senior Director, Market Access, Value & Economics, Intuitive
  • Dirk Abeel, Head of Global Sales, Reckitt Benckiser
  • William Chambers, Global Head of Transformation, Medtronic

Network with over 200+ commercial excellence, marketing and sales leaders from the worldโ€™s leading MedTech companies to make new contacts and develop lasting relationships.

โ€œA serious benchmark for other events- with burning Marketing and Sales topics embedded in a productive format that encourages peer-to-peer exchangeโ€ – Moritz Fischer, Director of International Marketing EMEA, Fresenius Medical Care

โ€œA highly interactive congress to discuss our common marketing and commercial challenges with a diverse group of companies- from established to new and those with a therapeutic or diagnostic focusโ€ – Christian Popp, Training and Development Director EMEA, Medtronic

To view the full agenda or to learn more about the event at MedForce, please visit the following link: https://bit.ly/312iCEU

For the latest news, be sure to follow MedForce on LinkedIn @MedForce Europe #MedForce20

 

Mental Health Programs: How To Know Which Therapy Is Right For You

Mental Health Programs: How To Know Which Therapy Is Right For You

Your mental health is important because this affects how you think, feel, and act. The state of your mental health can also determine how effectively you are able to handle stress, relate to other people, and make important life decisions. Your mental health is crucial at every stage of your life โ€“ from childhood until adulthood โ€“ which is why you should prioritize taking care of it.

If you have been experiencing mental health issues, donโ€™t fret as there are several mental health treatment programs. These options will help you improve your mental health regardless of how severe your mental health problem is or what kind of lifestyle you have right now. Completing these therapies will allow you to get back on track as soon as possible.

Hereโ€™s how you can determine which mental health therapy program is right for you:

1. Talk To A Professional First

There are several mental health therapy programs available today. Depending on the problem at hand, you can choose to participate in cognitive behavior therapy, a motivational interviewing group, or a wellness recovery action plan like Vertical Treatment Centers. All of these programs come with pros and cons but are targeted towards the same goal โ€“ to improve your mental health.

To save time and effort while choosing, get a professional assessment first. You should undergo an evaluation from a social worker, doctor, or psychiatrist who is certified under the American Society of Addiction Medicine. These professionals are trained and experienced enough to recommend therapies to treat substance use disorders.

This is an important step for you to explore all of your options and address any underlying mental health disorders. Itโ€™ll be easier for you to pick the right mental health therapy program when you talk to a professional as they will assess your mental health and substance abuse history in order to recommend the best plan of action.

2. Research Treatment Facilities

Getting a professional assessment can help you narrow down your options, but the final decision to choose a mental health therapy program will still come from you. To make this process easier for you, research the rehab centers youโ€™re considering and assess if any of these can provide the resources that you need.

Aside from substance abuse, itโ€™s possible that you might also have other clinical conditions such as chronic pain, severe anxiety and depression, and even trauma. If this is the case, the mental health therapy program you choose should offer solutions for dual-diagnosis patients.

Moreover, you should also learn about the accreditation of the facility. For you to truly recover from any mental health condition, the facility you choose should be licensed and certified by your state. Licenses and certifications will give you peace of mind that youโ€™re exerting time and effort for a therapy program that meets your stateโ€™s quality and state requirements.

3. Ask Questions

Researching online can give you an idea of how a specific facility operates, but you shouldnโ€™t stop there โ€“ you should exert time and effort to reach out to these facilities and ask as many questions as you can. This is a great way of knowing more about the facility and the therapy programs they offer, especially if these details arenโ€™t available online.

Depending on your preference, you can inquire whether or not a specific facility offers leisure activities or luxurious amenities. These facilities can improve your comfort when youโ€™re inside the facility, but they shouldnโ€™t be your sole consideration.

For you to choose the best mental health therapy program, the following factors are more important:

  • Are the therapy programs backed up by scientific evidence?

The therapy programs offered by a facility should be backed up by scientific evidence to warrant their efficacy. Paying for a therapy program that has zero success rates is a clear waste of time and money.

  • Does the facility meet the needs of each patient?

Mental health conditions such as anxiety, depression, and substance abuse are common today, but every patient is different. A mental health therapy program will have different effects on every patient.

When choosing a facility, make sure that it meets your unique needs as a patient. The facility and program should consider your age, cultural heritage, mental health history, history of trauma, and severity of substance abuse.

Youโ€™ll Reap What You Sow

Aside from picking the right mental health therapy program for yourself, make sure that you also try to be as open as possible during your sessions. Moreover, you should also set markers for change, do your work outside of your sessions and savor the entire process.

Completing a mental health therapy program isnโ€™t easy, but the rewards will surely be worth it in the end. Better mental health can be your ticket to experience less anxiety, improved moods, clearer thinking, and a greater sense of calm and inner peace.

Facility Inspiration Event at Interclean Amsterdam 2020 exhibition

Facility Inspiration Event at Interclean Amsterdam 2020 exhibition

On 12, 13 and 14 May facility and hospitality managers can once again take part in the Facility Inspiration Event at the Interclean Amsterdam international exhibition. The Facility Inspiration Event is being organised by Interclean and the facilities consultancy organisation, Atir.

Every day the programme will start with a networking lunch. This will be followed by a seminar programme with a keynote speaker and various sessions. As Marieke Weerts, managing partner at Atir, explains, “We have put together a programme for each day which links up with developments in a segment of the facilities sector. Our aim is to inspire facility and hospitality managers as to how they can respond even more effectively to future needs.”

Three days of inspiration per segment

The three days are devoted consecutively to Warehouse & Logistics (helping to optimise the supply chain), Leisure, Retail & Petrol (helping to optimise the customer experience in high traffic environments) and Real Estate & Corporate (helping to create the most ideal work and living environment). Keynote speakers have been arranged for each day who will outline the developments in the segment. For example, trend watcher and futurist Richard van Hooijdonk is scheduled to speak on Tuesday 12 May. He will give visitors an insight into the future of logistics and supply chain management by explaining, for example, how algorithms can help create a fully automatic supply chain and what facility management will look like in the world of automatic transport flows.

‘Perception of clean’ and neuromarketing

Every day, Josefien ten Have, who is a consumer psychologist at Consumatics, will be introducing visitors to the principles of neuromarketing. The focus will be on the influence of people’s subconscious to the ‘perception of clean’. During these sessions visitors will gain an insight into the factors which subconsciously contribute to the perception of clean surroundings and the cleaning behaviour of employees. She will provide specific, usable examples for each segment.

Circular world

In cooperation with the ZeroWaste Foundation, which is the driver for circular business operations, a tour is being organised during the Facility Inspiration Event to enable people to find out more about the various start-ups and scale-ups. Participants will be shown concrete examples of circular innovations which are intended specifically for facility management. During the tour visitors will be introduced to, for example, Flynther, a company that makes water-resistant packaging materials, such as waste boxes for hazardous waste produced in the healthcare sector. In addition, The Greenmachine, will present innovations which can be used to reduce waste, for example a dewatering machine which enables savings in terms of (work) space, time and waste costs.

Have we aroused your interest?

The Interclean Amsterdam international exhibition is taking place over four days from 10.00 to 17.30. Visitors can take part in the Facility Inspiration Event free of charge and without having to register in advance. The programme for the exhibition and the Facility Inspiration Event can be found on the website.

About Interclean

Established in Amsterdam in 1967, the world-leading Interclean events are organised by RAI Amsterdam. The Interclean brand represents products and solutions that tackle a wide range of challenges within the professional cleaning industry. Interclean Amsterdam 2020 will be the worldโ€™s largest professional cleaning and hygiene event, set to feature more than 900 exhibitors and attract around 35,000 visitors from 12-15 May 2020. For more information: www.intercleanshow.com

About RAI Amsterdam

Personal meetings continue to be a powerful form of communication, and exhibitions are the ideal medium for connecting worlds, people and markets. With a portfolio of top brands, RAI Amsterdam creates inspiring events that blend context, content and communities. The focus on quality and target group has made RAI Amsterdam the market leader in a significant number of sectors. Wherever in the world, an event may take place, RAI Amsterdamโ€™s focus is on generating business for exhibitors, visitors, sponsors and partners. For more information please visit www.rai.nl

 

The world’s first RIM’s medical platform is being created in Poland

The worlds first RIM's medical platform is being created in Poland

On January 7, 2020 consortium of Sages Sp. Z o.o. (Ltd.) and Warsaw University of Technology signed an agreement with Wroclaw Medical University (project leader) for the development of an open information platform called the Polish Medical Platform (PPM).

The project is being implemented with funds obtained under the Digital Poland Operational Programme (POPC.02.03.01-00-0008 / 17-00). Its purpose is to implement software which supports knowledge management and broad research potential, as well as, to provide data in the field of medicine, pharmacy, dentistry, public health, occupational health and safety, ergonomics, and health protection.

The platform will gather in one place, previously scattered information about: medical scientific publications, ongoing research, obtained patents, research equipment and profiles of scientists from the institutions implementing the project, and, in the future, from all institutions interested in cooperation. The portal’s key function will be the open access to publications and research data, which promotes broad access to knowledge, contributes to better promotion of achievements and seeking of partners for further cooperation, along with faster commercialization of research results. That what the Research Information Management (RIM) system offers: acquisition and aggregation, curation, and utilization of all metadata about research activities.

The project is implemented by eight institutions, including seven universities and one institute:

  • Wroclaw Medical University – project leader,
  • Medical University of Bialystok,
  • Medical University of Gda?sk,
  • Medical University of Silesia (Katowice),
  • Medical University of Lublin,
  • Pomeranian Medical University in Szczecin,
  • Medical University of Warsaw,
  • Nofer Institute of Occupational Medicine in Lodz.

The signed contract provides for the implementation of OMEGA-PSIR software, developed at the Institute of Computer Science, Warsaw University of Technology. So far, the software has been used in 20 universities and research institutes in Poland. The uniqueness of the currently implemented project lies in the simultaneous launch of the software in eight independent locations and the creation of a common platform, which will enable the integration of other research institutions with a similar research profile. This type of installation is the only such project in the world.

OMEGA-PSIR software is a fully functional RIM software combining the functions of CRIS systems (Current Research Information System โ€“ used in knowledge management), RPS (Research Profiling System โ€“ offers profiling of specialization of scientists and research institutions) and IR (Institutional Repositories โ€“ archiving of broadly defined scientific achievements of individuals and institutions).

Sages Sp. z o. o. (Ltd.) and the Institute of Computer Science, Warsaw University of Technology, have agreed on joint participation in the project, just like in several previous projects involving the implementation of OMEGA-PSIR.

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