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PRNews

Institut Marquès presents their studies on music and the beginning of life at the Massachusetts Institute of Technology

– Dr. Marisa López-Teijón, director of this internationally renowned center in Assisted Reproduction, has received the Ig Nobel Prize for Medicine

– The awards, held at Harvard University, recognize the most surprising and innovative scientific researches of the year

– Institut Marquès follows a line of state-of-the-art research on the effects of music on embryonic and fetal development

BOSTON, Sept. 19, 2017 /PRNewswire/ — Institut Marquès presented at the Massachusetts Institute of Technology (MIT) its scientific studies on the influence of music on embryonic and fetal development.


Dr. Marisa López-Teijón, director of Institut Marquès, Dr. Àlex García-Faura, scientific director of the center, and Lluís Pallarés, creator of the Babypod, accept their IG Nobel award.

Their work, published in the prestigious scientific magazine Ultrasound, has discovered how fetal hearing works, showing that fetuses hear from week 16 (when they measure 11 cm / 4 inches), as long as the sound comes to them from the mother’s vagina.

Dr. Marisa López-Teijón, director of Institut Marquès, Dr. Àlex García-Faura, scientific director of the center, and Lluís Pallarés, creator of the Babypod vaginal device, explained the conclusions of the study at MIT. Dr. Alberto Prats, Professor of Anatomy and Human Embryology of the Faculty of Medicine of the University of Barcelona, is also part of the research team.

This session at the Massachusetts Institute of Technology is part of the Ig Nobel Awards Ceremony, which recognize the most surprising and innovative scientific researches of the year.

Ig Nobel Prize for Medicine

Dr. Marisa López-Teijón has been awarded the Ig Nobel Prize for Medicine, the first one in Obstetrics in the 27-year history of the award.

The Ig Nobel ceremony is held at Harvard University and Massachusetts Institute of Technology, hosting prestigious scientists from around the world to present their studies to the public in a fun and enjoyable way.

At the ceremony, Dr. Marisa López-Teijón explained: “Institut Marquès is carrying out state-of-the-art research on how music impacts embryonic and fetal development.  

We have improved in vitro fertilization by applying musical vibrations inside the incubators in all our fertility clinics.

By inserting a speaker in the vagina of thousands of patients for the first time we have been able to communicate with the fetus. To achieve this we have created the Babypod. This is an FDA approved vaginal speaker that connects to the mobile phone.

Thanks to the Babypod, we have discovered how fetal hearing works: fetuses can barely hear noise outside the womb. The fetal ability to hear starts when the fetus only measures 4 inches or 11cm.  Until now medical literature could only confirm that fetuses heard from week 26 onwards. Fetuses responds just like babies, with speech and movements because they are learning to communicate. The myth of talking to your belly is over.”

According to Institut Marquès’ studies, we can now communicate with the fetus and neurologically stimulate it. Any kind of sensory stimulation is good,-and the earlier the better.

Music stimulates language learning. And as we see, learning can begin in the womb.

The Ig Nobel Prize represents a recognition by these prestigious universities for the research of Institut Marquès to improve assisted reproduction treatments.

Interesting links:

Music and fetal stimulation:

http://www.fertility-experiences.com/what-is-the-meaning-of-music/

http://www.fertility-experiences.com/the-story-of-a-discovery/

http://www.fertility-experiences.com/the-story-of-a-discovery-2-the-first-tests-continue/

http://www.fertility-experiences.com/the-story-of-a-discovery-3-the-scientific-research-starts/

http://institutomarques.com/en/scientific-area/response-fetus-vaginal-music-2/

http://www.institutomarques.com/pdf/ultrasound.pdf

Music and fertility:

http://www.fertility-experiences.com/music-enhances-in-vitro-fertilisation/

http://www.fertility-experiences.com/ivf-to-the-beat-of-the-music-we-have-made-our-embryos-dance/

Scientific studies:

http://institutomarques.com/en/scientific-area/

http://institutomarques.com/en/scientific-area/response-fetus-vaginal-music-2/

http://journals.sagepub.com/doi/abs/10.1177/1742271X15609367?journalCode=ultb

Babypod:

https://babypod.net/en/

Concerts for fetus and embryos

https://www.youtube.com/watch?v=SQNTqFRp09Q

https://www.youtube.com/watch?v=tQF5no3iLSg

Embriomobile:

http://institutomarques.com/en/observe-your-embryos-from-home/

More information: www.institutomarques.com and www.institutmarques.ie

Press contact United States:

kcontreras@webershandwick.com

Office: 617-520-7088
Mobile: 862-432-8436

Press contact Spain :

Institut Marquès Barcelona +34 93 285 82 16 

Mireia Folguera: mireia.folguera@institutomarques.com   +34 649 90 14 94

Estefanía Redondo: estefania.redondo@institutomarques.com   +34 661 20 83 85

Photo – https://mma.prnewswire.com/media/557034/Institut_Marques_Dr_Maris_Lopez_Teijon_director.jpg 
Video –  http://mma.prnewswire.com/media/557500/Institut_Marques.mp4 

PRNews

Asate AG: Great Honor for Swiss Therapist in America as Snoring and Sleep Apnoea Researcher Alex Suarez Receives Ig-Nobel Prize

BOSTON and ZURICH, Sept. 15, 2017 /PRNewswire/ — For millions of suffering people, a dream has finally come true: to be able to sleep without snoring. The unconventional innovation of successful Swiss Therapist, Alex Suarez (50), has solved the problem once and for all, and out of 9,000 nominations it has been selected to be awarded the “Ig Nobel Prize” at Harvard University. The Ig Nobel Prize, sometimes referred to as the Anti-Nobel Prize, is a satirical award, which honors scientific achievements “that first make people laugh, and then make them think” (Wikipedia). The Prize is announced in the Cambridge publication “Annals of Improbable Research”. In recent years, this award has enjoyed a high level of recognization amongst scientists.

Using the breathing techniques and training method developed by Alex Suarez called “Silent Sleep”, the troublesome problem of snoring can be solved naturally, easily, and in a playful way. The method used to strengthen and tighten the throat musculature and the connective tissue was developed by the Swiss relaxation coach over the course of 15 years. The idea for the Asate Method came to him during his own struggle with heavy snoring and sleep apnoea. Since conventional treatments were not providing him with any relief, the former dojo owner and instructor of Asian martial arts techniques, wanted to apply his knowledge of the yin and yang principle, biorhythms, tension and relaxation, as well as the careful consumption of resources, to create his very own therapy. Inspired by the Australian aboriginal didgeridoo, Suarez developed his own medicinal didgeridoo that is designed to strengthen, massage, and stimulate the connective tissue and musculature in the neck and mouth using targeted exercises.

This gentle alternative to medical devices or surgical intervention has achieved astonishing results that have been confirmed in international studies carried out by pulmonologists, sleep-researchers, and universities. The result of these studies show that in over 80% of cases, a marked improvement in sleeping without snoring can be achieved after only a few weeks using Silent Sleep training. The rapid success amongst the study participants has led to various stages of innovation involving the medical didgeridoo and has resulted in a device that is optimized for use in a therapeutic setting: the “Snadoo”. The significantly smaller instrument, which is made of plastic, can and should provide the user with additional amusement as they recover from their condition because how it is used and the corresponding mobile app are designed to be playful and fun.

More information is available at: http://www.asate.com

Contact:
Alex Suarez (until 09/20/17 in the USA)
alex@asate.com – 079-795-99-65

Aron Suarez
aron@asate.com – 079-839-03-85

PRNews

Frost & Sullivan Recognizes Acelity as a Leader in the Field with its new V.A.C.ULTA™ 4 Therapy System and V.A.C. VERAFLO CLEANSE CHOICE™ Dressing

Acelity’s innovative negative-pressure wound therapy system changes the game by enhancing delivery of four therapies on a single device

SANTA CLARA, California, Sept. 15, 2017 /PRNewswire/ — Based on its recent analysis of the negative-pressure wound therapy (NPWT) market, Frost & Sullivan recognizes Acelity with the 2017 North American Negative-Pressure Wound Therapy Product Leadership Award for its two new therapies: V.A.C.ULTA™ 4 Therapy System, which incorporates a fifth-generation software upgrade that provides delivery of four therapies on a single device, allowing physicians to treat various wounds with a single system, and V.A.C. VERAFLO CLEANSE CHOICE™ Dressing, which provides clinicians with a novel, adjunctive non-surgical option that may help clean large complex wounds when complete surgical debridement is not possible or appropriate.

Healthcare economies, such as the United States (US), are faced with shifting challenges, including rising operational costs at hospitals, staffing constraints, and cost burdens carried by care facilities for hospital-acquired infections. While US healthcare policies, along with value-based reimbursement models, are a clinical and economic driver in the wound care market, the need exists for wound care companies to integrate their treatment modalities into new care models that better track and manage chronic wounds across various care settings due to the shift from pay-for-service models to pay-for-performance and quality-of-care based payment models. The current chronic wound care market is also significantly fragmented because of the many ways a typical wound can be treated, including active healing dressings, advanced passive dressings, other unique energy- or mechanical-based solutions, and negative-pressure wound treatment systems (NPWT), including vacuum assisted-closure (V.A.C.®) therapy.

“Acelity is a leading provider of advanced wound care solutions,” said Patrick Riley, Principal Analyst at Frost & Sullivan. “The company pioneered NPWT, and its advanced V.A.C. VERAFLO™ Therapy combines the benefits of V.A.C.® Therapy and automated topical wound solution distribution and removal to help heal and prepare the wound for closure quickly and effectively. The new V.A.C.ULTA™ 4 Therapy System sets the benchmark with its capability to delivery four therapies through a single device.”

The four therapies include:

  • V.A.C. VERAFLO™ Therapy with Instillation, which automates alternating cycles of wound cleansing with a topical solution and V.A.C.® Therapy, allowing for wound cleansing and therapy to maintain a closed environment to enhance healing. V.A.C. VERAFLO™ Therapy is poised to become the new gold standard of NPWT, as studies have reported patient outcomes better than the current gold standard V.A.C.® Therapy.
  • Traditional V.A.C.® Therapy
  • ABTHERA™ Open Abdomen Negative Pressure Therapy, which provides negative-pressure therapy for temporary abdominal closure to help reduce edema and fluid, empowering primary fascial closure.
  • PREVENA™ Negative Pressure Incision Management Therapy, which provides NPWT therapy for closed incisions after a surgical procedure.

Furthermore, all four therapies utilize Acelity’s advanced SENSAT.R.A.C.™ Technology with EASYCLEAR PURGE™ which employs advanced software and algorithms in addition to multi-lumen technology that work together to monitor and regulate the set pressure continuously at the wound site, as well as helping reduce blockages. Acelity’s recently launched V.A.C. VERAFLO CLEANSE CHOICE™ dressing for use with V.A.C. VERAFLO™ Therapy helps loosen, solubilize, detach, and remove viscous wound exudate without surgical intervention, effectively preparing the wound for closure.

“Acelity’s software upgrade has also improved the ease-of-use factor for the V.A.C.ULTA™ 4 Therapy System,” said Riley. “Acelity has designed the interface to be similar to a mobile phone, with applications (apps) corresponding to each therapy for easy selection; thus, reducing the number of steps needed for therapy delivery.”

Acelity conducts hands-on training for clinicians, as well as transitioning training for customers moving to the new V.A.C.ULTA™ 4 Therapy System. The company also maintains customer, technical and clinical support teams that are committed to providing detailed support to customers for administrative questions, technological troubleshooting, and can give guidance on use of Acelity’s products.  

Acelity also recently launched V.A.C. VERAFLO CLEANSE CHOICE™ Dressing. When used with V.A.C. VERAFLO™ Therapy, Acelity’s negative pressure wound therapy and instillation (NPWTi-d) system, the dressing may provide rapid cleansing of wounds with the goal of augmenting the healing environment. The novel therapeutic dressing facilitates removal of thick wound exudate when surgical debridement is not possible or delayed, and offers prompt adjunctive wound cleansing for complex wounds.

In addition, Acelity has led the way in the next frontier of NPWT with its digital health offerings.   iOn RESULTS™ Remote Therapy Monitoring works in conjunction with the V.A.C.ULTA™ Therapy System to monitor the therapy units’ performance in the hospital setting. iOn PROGRESS™ Remote Therapy Monitoring delivers the first continuous monitoring and ready intervention for patients receiving negative pressure wound therapy in the home.

Due to Acelity’s commitment to improve patient outcomes through continuous technological innovation and outstanding customer support, Acelity has earned Frost & Sullivan’s 2017 North American Negative-Pressure Wound Therapy Product Leadership Award.

Each year, Frost & Sullivan presents this award to the company that has developed a product with innovative features and functionality that is gaining rapid market acceptance. The award recognizes the quality of the solution and the customer value enhancements it enables.

Frost & Sullivan Best Practices awards recognize companies in a variety of regional and global markets for demonstrating outstanding achievement and superior performance in areas such as leadership, technological innovation, customer service, and strategic product development. Industry analysts compare market participants and measure performance through in-depth interviews, analysis, and extensive secondary research to identify best practices in the industry.

About Acelity

Acelity L.P. Inc. and its subsidiaries are a global advanced wound care company that leverages the strengths of Kinetic Concepts, Inc. and Systagenix Wound Management, Limited. Available in more than 90 countries, the innovative and complementary ACELITY™ product portfolio delivers value through solutions that speed healing and lead the industry in quality, safety and customer experience. Headquartered in San Antonio, Texas, Acelity employs nearly 5,000 people around the world.

About Frost & Sullivan

Frost & Sullivan, the Growth Partnership Company, works in collaboration with clients to leverage visionary innovation that addresses the global challenges and related growth opportunities that will make or break today’s market participants. For more than 50 years, we have been developing growth strategies for the global 1000, emerging businesses, the public sector and the investment community. Contact us: Start the discussion.

Contact:

Estefany Ariza
P: 210.477.8469
F: 210.348.1003
E: Estefany.Ariza@frost.com

PRNews

Frost & Sullivan Applauds STANLEY Healthcare’s Design Innovation and Leadership in Addressing the Changing Needs of the Senior Living Industry

STANLEY Healthcare’s user-friendly, unobtrusive innovations address challenges in the market, making senior living communities tech savvy and future ready for implementing efficient senior care

SANTA CLARA, California, Sept. 7, 2017 /PRNewswire/ — Based on its recent analysis of the market for technology solutions for senior living communities, Frost & Sullivan recognizes STANLEY Healthcare with the 2017 Global Company of the Year Award. STANLEY Healthcare, a business unit of the Fortune 500 Company Stanley Black & Decker, is a leading solutions vendor for hospitals, health systems, and the senior living space. STANLEY Healthcare aims to expand its suite of solutions for the senior living market and deliver greater value to its clients in supporting their provision of senior care in an increasingly challenging environment.


STANLEY Healthcare receives the 2017 Global Senior Living Community Vendor Company of the Year Award

STANLEY Healthcare’s solutions serve several safety and security needs of senior living communities. These solutions include emergency call, wander management, staff security, facility security, and temperature monitoring. STANLEY Healthcare is the leader in fall management solutions, with over a million fall monitors installed over the past decade.

Going beyond its existing solutions and realizing the industry’s upcoming needs, STANLEY Healthcare is working to realize the ‘Smart Resident Room’. Integrating sensors in an Internet of Things fashion, the Smart Room concept will enable senior living communities to monitor residents unobtrusively while they carry on with their daily activities.

“Realizing the nature of technology and acknowledging the fast-changing pace of advancements, STANLEY Healthcare routinely partners with other technology companies whose solutions can integrate with its own to provide enhanced value for its customers,” said Industry Analyst Siddharth Shah at Frost & Sullivan. “It also partners with some of the WLAN and infrastructure providers to ensure its products and software work seamlessly with customers’ wireless infrastructure.”

An example of innovative technology founded on market needs is a wander management system using Bluetooth Low Energy (BLE) for wireless communication. “To lower the barriers to entry for wireless solutions, STANLEY Healthcare is moving towards using BLE solutions. Designing solutions that are appealing enough to attract residents is an approach that helps STANLEY Healthcare differentiate its solutions from others available in the senior living space,” said Shah.

Another key differentiator that distinguishes STANLEY Healthcare from the competition is its approach to customer care, including:

  • Product support services spanning the entire lifecycle of the solution.
  • The By Your Side™ customer support portal, which helps clients obtain answers to their queries, provides access to product documentation, and extends support for solving technical challenges.
  • 24/7 phone support, remote diagnostics, and on-site repair services.

Frost & Sullivan presents this award to the company that has leveraged competitive intelligence to execute successfully a competitive strategy that results in stronger market share, competitive brand positioning, and customer satisfaction.

Frost & Sullivan Best Practices Awards recognize companies in a variety of regional and global markets for demonstrating outstanding achievement and superior performance in areas such as leadership, technological innovation, customer service, and strategic product development. Industry analysts compare market participants and measure performance through in-depth interviews, analysis, and extensive secondary research to identify best practices in the industry.

About STANLEY Healthcare

STANLEY Healthcare provides over 5,000 acute care hospitals and 12,000 long-term care organizations with enterprise solutions that create a safe, secure and efficient healthcare experience across life’s stages. The STANLEY Healthcare solution set enables customers to achieve organizational excellence and superior care in critical areas: Patient/Resident Safety, Security & Protection, Environmental Monitoring, Clinical Operations & Workflow and Supply Chain & Asset Management. These solutions are complemented by STANLEY Healthcare’s By Your Side™ Lifetime Customer Care commitment to ensure that every customer achieves success and realizes the full value of their investment, through consulting, training, implementation and integration services. STANLEY Healthcare is proud to be part of Stanley Black & Decker, Inc. For more information, visit stanleyhealthcare.com. Follow STANLEY Healthcare on Facebook, Twitter, LinkedIn and YouTube.

About Frost & Sullivan

Frost & Sullivan, the Growth Partnership Company, collaborates with clients to leverage visionary innovation that addresses the global challenges and related growth opportunities that will make or break today’s market participants. For more than 50 years, Frost & Sullivan has been developing growth strategies for the global 1000, emerging businesses, the public sector, and the investment community. Contact us: Start the discussion.

Contact:

Claudia Toscano
P: 210.477.8417
F: 210.348.1003
E: claudia.toscano@frost.com

PRNews

PQ Bypass Earns Frost & Sullivan’s European Technology Innovation Award for Its Proprietary DETOUR System for Percutaneous Bypass

Novel technology enables a new, minimally invasive treatment for patients suffering from extremely long peripheral artery blockages

LONDON, Aug. 31, 2017 /PRNewswire/ — Frost & Sullivan is pleased to recognize PQ Bypass with the 2017 European PAD Interventions Technology Innovation Award. PQ Bypass’ DETOUR System is a minimally invasive technology that enables physicians to re-direct, or detour, blood flow around extremely long blockages in the upper leg arteries to restore blood flow to the lower leg and foot.

“PAD is a potentially fatal condition that affects more than 200 million people worldwide—3 to 12% of the global population. PQ Bypass’ proprietary DETOUR System is a promising, innovative approach for patients with extremely long lesions whose current treatment options are not ideal,” said Frost & Sullivan Best Practices Analyst, Norma Vela. “We anticipate rapid, widespread technology adoption once the DETOUR System launches commercially. The global market potential for treating this type of advanced peripheral arterial disease is significant, and PQ Bypass has first-mover status in the space.”

Extremely long blockages in the leg arteries, especially those that are greater than 20 centimeters, are challenging to treat. Historically, physicians have treated these blockages with open bypass surgery (fem-pop bypass), which has the benefit of durability, however, it is associated with an increased risk of complications, longer hospital stays, and prolonged rehabilitation. More recently, minimally-invasive technologies have emerged that go through blockages. These technologies work very well on shorter blockages; however, they have not been as effective on these longer blockages as open surgery.

The DETOUR System is designed to deliver the durability advantages of open bypass surgery with a minimally-invasive approach. During a DETOUR procedure, a pathway is created by crossing from the SFA into the femoral vein and back into the artery that allows DETOUR stent grafts to be placed in a continuous line. The new path through the stent grafts re-directs oxygen-rich blood around the blockage and restores blood flow to the lower leg and foot of the patient.

“With an increased focus on value-based and patient-centered medicine, surgical advancements that minimize trauma to patients, reduce length of hospital stay and recovery times are critical global needs,” said Richard Ferrari, Chairman of the Board of PQ Bypass. “We designed the DETOUR System to be a transformative step forward in how physicians treat extremely long peripheral artery disease.”

In March 2017, PQ Bypass received CE Mark approval for the DETOUR System and is planning a pivotal investigational device exemption study to support premarket approval from the US Food and Drug Administration (FDA). The clinical results of the DETOUR I trial conducted in Europe were promising, demonstrating excellent safety and effectiveness with patency results of 84.7% at 6 months.

Each year, Frost & Sullivan presents this award to a company that has developed a pioneering technology that enhances current products and develops newer products and applications. The award recognizes the high market acceptance potential of the recipient’s technology.

Frost & Sullivan Best Practices Awards acknowledge companies in a variety of regional and global markets for demonstrating outstanding achievement and superior performance in areas such as leadership, technological innovation, customer service, and strategic product development. Industry analysts compare market participants and measure performance through in-depth interviews, analysis, and extensive secondary research to identify best practices in the industry.

About PQ Bypass

PQ Bypass, Inc. is a Silicon Valley-based medical device company working to transform the treatment of long-segment peripheral artery disease with minimally-invasive endovascular solutions.

PQ Bypass is operated by recognized leaders in the medical device industry. Our executive team members have held senior leadership positions at companies including Medtronic, Abbott, Johnson & Johnson, and Stryker and also have extensive experience developing medical devices for startups such as Evalve, Access Closure, Avinger, and DVI.

The underlying technology and technique used in the percutaneous PQ DETOUR procedure were co-developed by two world-renowned cardiologists and innovators, Dr. James Joye and Dr. Richard Heuser, who are recognized experts in PAD.

The PQ Bypass technology platform is not available for sale in the US. For more information, please visit www.pqbypass.com.

About Frost & Sullivan

Frost & Sullivan, the Growth Partnership Company, collaborates with clients to leverage visionary innovation that addresses the global challenges and related growth opportunities that will make or break today’s market participants. For more than 50 years, Frost & Sullivan has been developing growth strategies for the global 1000, emerging businesses, the public sector, and the investment community. Contact us: Start the discussion.

PRNews

Ondine’s President and CTO receives 2017 Clinical Research Excellence Award at Global IPA Conference

VANCOUVER, British Columbia, Aug. 11, 2017 /PRNewswire/ — Ondine Biomedical Inc. is pleased to announce that its President and Chief Technology Officer, Dr. Nicolas Loebel, was the 2017 recipient of the International Photodynamic Association’s CLINICAL PDT RESEARCH EXCELLENCE AWARD. The award was presented at the World Congress held in Coimbra, Portugal. The Coimbra World Congress was the 16th conference held by the International Photodynamic Association, marking 32 years of this global meeting. The IPA World Congresses, held every two years, are the leading PDT meetings bringing together members of the global photodynamic community in order to advance scientific and clinical research relating to photodiagnosis and photodynamic therapies.

“I am delighted to see that Dr. Loebel was duly recognized by his peers for his clinical advancement of antimicrobial photodynamic therapy and track record of research excellence. This IPA recognition is well deserved.” stated Professor Michael Wilson, inventor of antimicrobial photodynamic therapy. Professor Wilson is Emeritus Professor of Microbiology at the Eastman Dental Institute in the Faculty of Medical Services of University College London (UCL). Professor Wilson was the first to successfully treat complex biofilm infections using antimicrobial PDT, demonstrating the potency of this technology against multidrug-resistant pathogens.

Ondine Biomedical Inc. is a Canadian medical device company developing and commercializing antimicrobial photodynamic therapies to treat and prevent multidrug resistant infections. Dr. Nicolas Loebel and his team at Ondine Research Laboratories have developed 5 antimicrobial photodynamic products, including Periowave™ (oral infections), Sinuwave™ (sinus infections), MRSAid™ (nasal decolonization), Steriwave™ (skin infections) and Exelume™ (VAP reduction), positioning Ondine as the global leader in Photodisinfection based therapies.  More than 300,000 patients have been treated with Ondine’s technologies globally, demonstrating excellent clinical outcomes and safety profiles. For more information, please visit: www.ondinebio.com

Source: Ondine Biomedical Inc.

PRNews

Frost & Sullivan Acclaims Shimadzu for Delivering a Product Line of Versatile and Innovative Radiography Solutions

Shimadzu’s products utilize advanced robotic capabilities and next-generation digital imaging technologies

LONDON, Aug. 3, 2017 /PRNewswire/ — Based on its recent analysis of the general radiography market, Frost & Sullivan recognizes Shimadzu Corporation with the 2017 Global Frost & Sullivan Award for Product Line Strategy Leadership. Constant innovations and upgrades to Shimadzu’s radiography product portfolio have ensured that the products stay relevant and in high demand in an evolving radiography market. Its comprehensive product range enhances automation, efficiency, image quality, and overall clinical value by enabling flexible positioning, reduced radiation dose, and versatility in viewing bone and soft tissue images.

Shimadzu has the entire range of general radiography solutions, from fixed ceiling-mounted to floor-mounted systems and mobile X-ray solutions, with or without one to two arms. These are all available all in entry-level to high-end configurations. In 2016, it introduced new technologies such as digital multi-slice tomography with flexible positioning to offer a view of oblique cross sections of the spine and hip joints. Other products include:

  • SONIALVISION G4, a fluoroscopy product with multi-functionality features
  • RADspeed Pro EDGE package, a high-performance general radiography equipment
  • MobileDaRt Evolution MX7 Version, mobile X-ray with digitization features.

RADspeed Pro EDGE and MobileDaRt Evolution MX7 have already been adopted by more than 100 hospitals worldwide within a year of their introduction.

“In response to customer demand, Shimadzu introduced a sophisticated, remote-controlled, auto-positioning feature in the RADspeed Pro EDGE package. This feature helps the radiographer effortlessly position the tube and fine-tune this positioning to improve patient safety and reduce radiation dose,” said Frost & Sullivan Consultant Poornima Srinivasan. “Similarly, it incorporated removable grids to lower radiation exposure during pediatric imaging, and a dose area product meter on the collimator to measure the dose of radiation the patient is exposed to.”

Shimadzu’s products have proven their utility in guiding hospitals towards the era of value-based healthcare. They achieve that by incorporating a host of novel features and technologies.

  • The RADspeed Pro EDGE employs cutting-edge technologies like tomosynthesis, speed stitch, and dual energy subtraction. Tomosynthesis combines cone-beam computed tomography (CT) reconstruction with digital image processing so that any number of cross-sectional images can be obtained. The systems also incorporate ‘T-smart,’ the metal artifact reduction technology that decreases metal artifacts in orthopedic patients. Additionally, it uses speed stitch technology, which combines multiple images that are captured while the X-ray tube is in motion at various angles. Finally, its dual energy subtraction, imaging algorithm, couples with low and high voltages to offer images of soft tissue and bone images separately.
  • SONIALVISION G4 is capable of a wide range of examinations and is ideal for inter-departmental shared services. The field of view (FOV) flat panel detector (FPD) is available in five sizes and provides an extensive imaging area, ultra-high definition and dynamic images, less radiation exposure, a ceiling-mounted telescopic arm, and a wall stand with a portable FPD. It incorporates technologies such as:
    • The SUREengine-Advance, an image processing technology that delivers quality fluoro and radiography images
    • SLOT Advance, an optimal technology for long-view images with a minimal X-ray dose
    • T-smart, the latest tomosynthesis technology that aids in iterative reconstruction with metal artifact suppression
  • The MobileDaRt Evolution MX7 Version incorporates a large LCD monitor and LED collimator light that increases brightness up to 40% and saves electricity by 80% when compared to its competing products. It also has a user-friendly design with wireless capability, which allows it to extend its scope of application.

“Shimadzu has leveraged the expertise of key opinion leaders (KOLs), designed training and educational programs, expanded geographically, and made the most of cross-selling opportunities in line with its business goals,” noted Ms. Srinivasan. “Additionally, it has partnered with universities to optimize the existing systems and develop further innovations and efficiencies. Shimadzu’s discussions with international channels, and focus on gathering input from healthcare professionals have played a huge role in its development of unique products and provision of a rich customer experience.”

Each year, Frost & Sullivan presents this award to the company that has developed a comprehensive product line that caters to the breadth of the market it serves. The award recognizes the extent to which the product line meets customer base demands, the overall impact it has in terms of customer value, as well as increased market share.

Frost & Sullivan Best Practices awards recognize companies in a variety of regional and global markets for demonstrating outstanding achievement and superior performance in areas such as leadership, technological innovation, customer service, and strategic product development. Industry analysts compare market participants and measure performance through in-depth interviews, analysis, and extensive secondary research to identify best practices in the industry.

About Shimadzu Corporation

Shimadzu Corporation has remained committed to commercializing cutting-edge technology and providing it to customers in a wide array of industries for more than 140 years. Our brand statement, “Excellence in Science”, reflects our desire and attitude to diligently respond to customers’ requirements by offering superior, world-class technologies indispensable for analytical and measuring instruments, medical systems, aircraft equipment and industrial machinery in the area of human health, safety and security of society and advancement of industry. In the ever-changing landscape of challenges of society, Shimadzu aims to partner with customers to meet their needs with unique technologies and solutions.

About Frost & Sullivan

Frost & Sullivan, the Growth Partnership Company, works in collaboration with clients to leverage visionary innovation that addresses the global challenges and related growth opportunities that will make or break today’s market participants. For more than 50 years, we have been developing growth strategies for the global 1000, emerging businesses, the public sector, and the investment community. Contact us: Start the discussion.

Contact:

Ana Arriaga
P: 210.247.3823
F: 210.348.1003
E: ana.arriaga@frost.com

PRNews

Frost & Sullivan Lauds CytoSorbents for Leading the Critical Care Immunotherapy Segment with its Novel Blood Purification Solution, CytoSorb®

By controlling dangerous inflammation, CytoSorb® is enabling superior outcomes in critically-ill patients, with reduced overall costs of intensive care in its sights

LONDON, Aug. 2, 2017 /PRNewswire/ — Based on its recent analysis of the blood purification market, Frost & Sullivan recognizes CytoSorbents Corporation with the 2017 Global Frost & Sullivan Award for Product Leadership. CytoSorbents’ deceptively simple yet powerful blood purification therapy, CytoSorb®, helps critical care physicians and heart surgeons control deadly inflammation in their patients. CytoSorb® actively reduces circulating cytokines, toxins, and other substances in blood that feed and perpetuate uncontrolled inflammation in a diverse set of medical emergencies such as sepsis, infection, trauma, cardiac surgery, and liver failure. Its ultimate aim is to prevent a patient from being killed by his or her own out-of-control immune response.

“There were many factors that led to our selection of CytoSorb® for this year’s Global Product Leadership Award,” said Frost & Sullivan Research Analyst Aish Vivek. “Among the most important was the recognition that this innovative product is surprisingly well-positioned to help solve two long-standing, difficult, and tightly linked fundamental problems with hospital medicine today. These include the high rates of death from common critical illnesses such as sepsis that have no approved treatment, and the resulting staggering costs and losses in critical care that are financially crippling hospital networks and healthcare systems throughout the world.”

“Further strengthening CytoSorb’s position is the scarcity of viable competition in the lucrative and vast global critical care and cardiac surgery markets, the strong physician usage and revenue growth, and the external validation from well-respected industry partners, such as Fresenius Medical Care and Terumo Cardiovascular, and government funding agencies.  As a high margin, single-use product that works with existing blood pumps in hospitals, CytoSorb® also has an attractive business model that is expected to drive early and significant profitability of the company.”

“CytoSorb® has taken blood purification as a means to control inflammation to the next level, with its patented blood compatible, porous polymer bead technology,” concluded Aish Vivek. “This best-of-breed solution is approved in the European Union and has been used in more than 23,000 treatments to help save many lives across 44 countries.  As the clinical experience and scientific publications continue to grow, we predict that CytoSorbents, through CytoSorb®, will solidify its leadership in critical care and cardiac surgery, with expansion into other promising fields such as cancer immunotherapy, and treatment of chronic illness. We are also excited to follow along as CytoSorbents initiates a registration trial later this year that targets U.S. FDA approval.”

Overall, for positioning itself strongly with its CytoSorb® therapy and serving a wide array of applications, Frost & Sullivan is pleased to present CytoSorbents with the 2017 Global Frost & Sullivan Award for Product Leadership in the blood purification market.

Each year, Frost & Sullivan presents this award to the company that has developed a product with innovative features and functionality, gaining rapid acceptance in the market. The award recognizes the quality of the solution and the customer value enhancements it enables.

Frost & Sullivan Best Practices Awards recognize companies in a variety of regional and global markets for demonstrating outstanding achievement and superior performance in areas such as leadership, technological innovation, customer service, and strategic product development. Industry analysts compare market participants and measure performance through in-depth interviews, analysis, and extensive secondary research to identify best practices in the industry.

About CytoSorbents Corporation

CytoSorbents Corporation (NASDAQ: CTSO) is a leader in critical care immunotherapy, specializing in blood purification. Its flagship product, CytoSorb®, is approved in the European Union with distribution in 44 countries worldwide, as a safe and effective extracorporeal cytokine adsorber, designed to reduce the “cytokine storm” or “cytokine release syndrome” that could otherwise cause massive inflammation, organ failure and death in common critical illnesses such as sepsis, burn injury, trauma, lung injury, complications of surgery, cancer immunotherapy, and pancreatitis. These are conditions where the risk of death is extremely high, yet no effective treatments exist. CytoSorb® is also being used during and after cardiac surgery to remove inflammatory mediators, such as cytokines and free hemoglobin, which can lead to post-operative complications, including multiple organ failure. In 2017, the company plans to initiate a pivotal REFRESH 2 trial intended to support U.S. FDA approval.  CytoSorb® has been used safely in more than 23,000 human treatments to date.

CytoSorbents’ purification technologies are based on biocompatible, highly porous polymer beads that can actively remove toxic substances from blood and other bodily fluids by pore capture and surface adsorption. Its technologies have received non-dilutive grant, contract, and other funding in excess of $19 million from DARPA, the U.S. Army, the U.S. Department of Health and Human Services, the National Institutes of Health (NIH), National Heart, Lung, and Blood Institute (NHLBI), U.S. Special Operations Command (SOCOM) and others. The Company has numerous products under development based upon this unique blood purification technology, protected by 32 issued U.S. patents, multiple international patents, and many applications pending worldwide.  Products under development include CytoSorb-XL™, HemoDefend™, VetResQ™, ContrastSorb, DrugSorb, and others.  Visit www.cytosorbents.com and www.cytosorb.com

About Frost & Sullivan

Frost & Sullivan, the Growth Partnership Company, works in collaboration with clients to leverage visionary innovation that addresses the global challenges and related growth opportunities that will make or break today’s market participants. For more than 50 years, we have been developing growth strategies for the global 1000, emerging businesses, the public sector, and the investment community. Contact us: Start the discussion.

Contact:

Aish Vivekanandan
Phone: 210-477-8495
Email: aish.vivekanadan@frost.com

PRNews

Frost & Sullivan Commends Credence ID’s Rollout of CredenceTAB(TM), a Biometric Tool that Combines Document Reading and Biometric Enrollment and Verification in a Portable Device

Credence ID’s unique product suite offers convenience, portability, and customization to satisfy a wide range of identification projects

SANTA CLARA, California, Aug. 1, 2017 /PRNewswire/ — Based on its recent analysis of the mobile biometrics and credential reading market, Frost & Sullivan announced today the recognition of Credence ID for its 2017 Global New Product Innovation Award. In May 2017, Credence ID introduced CredenceTAB, a 10-inch tablet that combines the functionalities of an eDocument reader, high-resolution camera, fingerprint scanner, machine readable zone (MRZ), and a smart card reader in a single handheld device for the biometric ID industry. The solution was developed in line with the company’s vision to deliver enrollment and identification solutions to facilitate programs that provide benefits to underdeveloped and under-documented populations worldwide. With its portability and connectivity through Wi-Fi, Bluetooth, and mobile networks, the CredenceTAB greatly aids the national ID programs of various governments.

CredenceTAB and its related software development kit (SDK) enjoy a plethora of application opportunities across both government and commercial applications. The solution’s fingerprint scanner uses a FAP-30 sensor that enables fingerprint capture in all lighting conditions. The sensor is based on a light emitting sensor (LES) optical technology, which captures the optical image of the fingerprint on a thin film transistor to generate a PIV class fingerprint image. Additionally, Credence ID supports facial recognition and barcode reading by embedding two high-resolution cameras in CredenceTAB.

“CredenceTAB provides broad flexibility to its customers through its multi-functional, portable, battery-powered solution,” said Frost & Sullivan Industry Analyst Ram Ravi. “Credence ID has leveraged years of experience in designing, engineering, and manufacturing mobile identification devices to create this purpose-built, competitively-priced product. Furthermore, as they are built on an open development platform, Credence ID’s products are configurable and aid complete customization of the biometric device.”

Significantly, Credence ID’s main biometric solutions, Trident®, CredenceONE™, CredenceONE-MRZ™, and CredenceTAB, boast user friendliness and multi-modal product features that far exceed the accuracy and speed of the latest consumer devices.

  • Trident is a tri-biometric platform encompassing a dual-iris scanner, an industry-leading FAP 45 fingerprint sensor, and a high-resolution camera to capture facial images. The solution employs a long-life lithium ion battery that extends duty cycles.
  • CredenceONE’s robust, compact mobile chipset enables multiple identity-based solutions by using three sensors for scanning smart cards, faces, and fingerprints.
  • CredenceONE-MRZ and CredenceTAB feature four sensors on-board. Additionally, these solutions have a completely integrated smart card reader system (contact and contactless), a MRZ scanner, a facial recognition camera, and an enterprise-class fingerprint sensor.

Credence ID’s product design strategy has augmented its success, particularly in government and civil ID programs, which, in turn, has eased the company’s entry into commercial Know your Customer (KYC) applications.

“Credence ID has established an impressive clientele of top-tier value-added resellers and solution providers that build, manage, and support government and civil ID programs and applications,” noted Ravi. “By using the Android OS, Credence ID endows its partners with the freedom to create an array of intuitive applications. Its knack for industrial design and innovation, backed by continuous product improvement and customer support, has established it as a trustworthy supplier of mobile biometric solutions to government and civil ID applications.”

Each year, Frost & Sullivan presents this award to the company that has developed an innovative element in a product by leveraging leading-edge technologies. The award recognizes the value-added features/benefits of the product and the increased return on investment (ROI) it provides to customers, which, in turn, raises customer acquisition and overall market penetration potential.

Frost & Sullivan Best Practices Awards recognize companies in a variety of regional and global markets for demonstrating outstanding achievement and superior performance in areas such as leadership, technological innovation, customer service, and strategic product development. Industry analysts compare market participants and measure performance through in-depth interviews, analysis, and extensive secondary research to identify best practices in the industry.

About Credence ID

Headquartered in Emeryville, California, Credence ID was formed by like-minded business leaders focused on providing non-reputable biometric identities, especially to marginalized populations. The company’s personnel include experts in the field of biometrics and advanced mobile technologies. The Credence ID product line offers mobile biometric solutions and credential reading. With the industry at the crossroads of mobile and biometric technologies, Credence ID’s product line is perfectly aligned to capitalize on this trend. The company’s product suite includes features such as lower costs, better performance, advanced ergonomics, and complete customization.

About Frost & Sullivan

Frost & Sullivan, the Growth Partnership Company, collaborates with clients to leverage visionary innovation that addresses the global challenges and related growth opportunities that will make or break today’s market participants. For more than 50 years, Frost & Sullivan has been developing growth strategies for the global 1000, emerging businesses, the public sector, and the investment community. Contact us: Start the discussion.

Contact:

Estefany Ariza
P: 210.477.8469
E: estefany.ariza@frost.com

Photo – https://mma.prnewswire.com/media/540828/Credence_Award_Logo.jpg

PRNews

Frost & Sullivan Acclaims CGI’s Advanced Genomic & Biomarker Technologies That Drive Industry Innovation in Support of Precision Cancer Treatment

CGI’s technologies provide valuable insights across cancer diagnostics through the accurate and sensitive quantitation of clinically relevant genomic signatures & biomarkers from both blood and tissue samples

SANTA CLARA, California, July 26, 2017 /PRNewswire/ — Based on its recent analysis of the precision oncology industry, Frost & Sullivan recognizes Cancer Genetics, Inc. (CGI or the Company) with the 2017 North American Frost & Sullivan Award for Technology Innovation. CGI’s leading-edge technology platforms and comprehensive menu of diagnostic services enhance precision oncology by enabling earlier cancer detection, improving treatment management, and aiding the development of novel cancer therapies. The Company’s genomic products and services not only present diagnostic, prognostic, and theranostic information for routine clinical care, but also facilitate and accelerate drug development programs seeking to deliver targeted, more effective and safer drugs to market more quickly. With its comprehensive suite of both off-the-shelf and proprietary tests, technology-agnostic approach, global infrastructure, and extensive research collaborations, CGI is at the forefront of enabling precision medicine in oncology globally, from bench to bedside.

“CGI has a wide variety of assays for genomic and immuno-oncology related biomarkers, applicable across several therapeutic areas, including hematological malignancies, solid tumors, and hereditary cancers,” said Frost & Sullivan Research Analyst Vandana Iyer. “The Company offers a broad range of laboratory services that provide critical genomic and biomarker information for patient care and for clinical trials being performed by biotech and pharmaceutical companies. CGI’s recent launches of cutting edge tests, its ability to partner with innovative companies, and its extensive research collaborations with leading academic institutions and cancer centers are a testament to the value and depth of CGI’s commitment to driving industry innovation.”

Some of CGI’s prominent and recently launched technologies include:

  • Complete::IO™ is a unique and in-depth flow cytometry panel supporting informed therapeutic decisions and assessment of potential toxicities for novel immuno-oncology (IO) therapies in blood cancers and solid tumors.
  • Focus::Oncomine™ is capable of simultaneously testing DNA and RNA, enabling the detection of various types of genomic alterations in a single workflow that requires minimal sample quantities and boasts a rapid turnaround time. The Focus::Oncomine™ assay can detect thousands of clinically and pharmacologically relevant biomarkers in solid tumors, making it a valuable tool for clinicians and biopharma.
  • Focus::Lymphoma™ is the most comprehensive next generation sequencing (NGS) panel for B-cell lymphomas in the field.  Focus::Lymphoma™, sequences 220 clinically-actionable genes, allowing clinicians to determine the most effective treatment management for patients. Focus::Lymphoma™ is also offered to biotech and pharmaceutical companies to power efficient clinical trials focused on B-cell lymphomas.
  • Focus::Renal™ is a highly-sensitive NGS panel that provides thorough information for the diagnosis, prognosis and therapy selection in renal cancers.  In a single test, Focus::Renal™ is able to detect mutations in 76 renal cancer-related genes, as well as genome-wide copy number changes, and critical single nucleotide polymorphisms (SNPs). Focus::Renal™ is the only NGS panel of its type, as it is disease-focused, and has been developed through collaboration with leading cancer centers and academic institutions, including MSKCC, Cleveland Clinic, Huntsman Cancer Center at University of Utah, and University Hospital of Paris.
  • Liquid::Lung-cfDNA™ is a CLIA-validated, multi-gene NGS panel for lung cancer liquid biopsies. The test can detect lung tumor-derived cell-free DNA (cfDNA) obtained from a single blood draw, and analyzes frequently-mutated SNPs and short indels in 11 genes with significant clinical relevance to non-small cell lung cancer (NSCLC). This groundbreaking assay is highly sensitive, with a limit of detection (LOD) as low as 0.05% or 1 mutant copy of DNA in a background of 2,000 wild-type copies of DNA.
  • Focus::HERSite™ is a hereditary cancer test that focuses on breast and ovarian cancers. The test analyzes the 16 genes most commonly associated with breast and ovarian cancers and provides in-depth coverage of BRCA1 and BRCA2.
  • Oncomine Dx Target Test is the first NGS-based companion diagnostic (CDx) test that simultaneously screens tumor samples for biomarkers associated with 3 FDA-approved therapies for non-small cell lung cancer (NSCLC). CGI is one of the first laboratories, and one of only three in the United States, to offer the Oncomine Dx Target Test.

CGI has established a global footprint with a presence in the United States, India, and China. The Company’s infrastructure, which has been developed through strategic acquisitions, and its unique business model, which incorporates routine clinical testing for cancer patients and fee-for-service solutions for biotech and pharmaceutical companies, have positioned it uniquely for diversified growth and access to the oncology community. These factors have supported the Company’s successful development of a durable business model through which to commercialize its oncology programs and testing capabilities.

“CGI is a technology-agnostic company with comprehensive diagnostic capabilities utilizing various platforms, including next generation sequencing, fluorescence in situ hybridization, immunohistochemistry, microarrays, RT-PCR, and flow cytometry. The Company boasts full NGS capabilities with both Illumina and Thermo Fisher platforms, offering a mix of proprietary panels and off-the-shelf assays,” noted Iyer. “CGI has several ongoing research collaborations with leading oncologists and cancer centers in both solid tumors and hematological malignancies, including kidney cancer, leukemia, non-Hodgkin’s lymphoma, and HPV-associated cancers. The Company constantly strives for diversity and innovation, and has successfully achieved a balance between the two.”

Each year, Frost & Sullivan presents this award to the company that has demonstrated uniqueness in developing and leveraging new technologies, which significantly impact both the functionality and the customer value of new products and applications. The award lauds the high R&D spend towards innovation, its relevance to the industry, and the positive impact on brand perception.

Frost & Sullivan Best Practices awards recognize companies in a variety of regional and global markets for demonstrating outstanding achievement and superior performance in areas such as leadership, technological innovation, customer service, and strategic product development. Industry analysts compare market participants and measure performance through in-depth interviews, analysis, and extensive secondary research to identify best practices in the industry.

ABOUT CANCER GENETICS, INC.

Cancer Genetics, Inc. is a leader in enabling precision medicine in oncology from bench to bedside through the use of oncology biomarkers and molecular testing. CGI is developing a global footprint with locations in the US, India and China. We have established strong clinical research collaborations with major cancer centers such as Memorial Sloan Kettering, The Cleveland Clinic, Mayo Clinic, Keck School of Medicine at USC and the National Cancer Institute.
The Company offers a comprehensive range of laboratory services that provide critical genomic and biomarker information. Its state-of-the-art reference labs are CLIA-certified and CAP-accredited in the US and have licensure from several states including New York State.

For more information, please visit or follow CGI at:

Internet: www.cancergenetics.com
Twitter: @Cancer_Genetics
Facebook: www.facebook.com/CancerGenetics
Media Contact:
Panna Sharma
Cancer Genetics, Inc.
Tel: 201-528-9200
Email: panna.sharma@cgix.com

Investor Relations Contact:
Richard Moyer
Cameron Associates
535 Fifth Ave., New York, NY 10017
Tel: 212-554-5466
Email: richard@cameronassoc.com

About Frost & Sullivan

Frost & Sullivan, the Growth Partnership Company, works in collaboration with clients to leverage visionary innovation that addresses the global challenges and related growth opportunities that will make or break today’s market participants. For more than 50 years, we have been developing growth strategies for the global 1000, emerging businesses, the public sector, and the investment community. Contact us: Start the discussion.

Contact:

Andrea Steinman
P: 210.477.8425
F: 210.348.1003
E: andrea.steinman@frost.com