Category Archives: Industry: Healthcare

Healthcare is an ever evolving industry, and field. These Press Releases, will keep you up to date on the newest, greatest, best, solutions available.

Vuja De Sciences Announces the Appointment of Two New Board Members


“Targeting metastatic progression has been my passion for over 20 years and the team at Vuja De stands poised to rapidly translate new findings from its metastasis drug screens to effective drugs for the primary unmet need for cancer patients”, said Dr. Khanna.

Vuja De Sciences (“Vuja De”), a biotechnology startup dedicated to developing cancer metastasis treatments that prevent cancer progression and recurrence, today announced the appointments of Chand Khanna, DVM, PhD, DACVIM (Onc), and Dr. Lee Helman, MD, to its Board of Directors. Rick Lampe, Co-founder and CEO of Vuja De said, “We are delighted to welcome Chand and Lee as new directors. They will be of great help in advancing our unique approach to the discovery and development of metastatic progression targeting cancer treatments in osteosarcoma and other cancers.” Dr. David Warshawsky, Vuja De’s Founder and Chairman of the Board added: “I am confident that their leadership will have a highly meaningful impact on Vuja De’s ability to translate our core anti-metastasis drug discovery platform to ground-breaking therapies against cancer progression and to our success in building a strong and leading company in the fight against cancer.”

Vuja De has been collaborating with Dr. Chand Khanna, Chief Science Officer of Ethos Veterinary Health and President of Ethos Discovery. Through this interaction VuJa De and Ethos have an innovative collaborative plan and path for metastasis-focused drug development that includes clinical trials in pet dogs with cancer (i.e. comparative oncology). “I am delighted to join the leadership at Vuja De. Targeting metastatic progression has been my passion for over 20 years and the team at Vuja De stands poised to rapidly translate new findings from its metastasis drug screens to effective drugs for the primary unmet need for cancer patients,” said Dr. Khanna.

Dr. Lee Helman stated: “I am delighted to join the Vuja De board and to work with the team to do whatever is needed to help bring treatments that prevent cancer progression and recurrence to patients with osteosarcoma and other cancers.”

“Ethos Veterinary Health is excited and highly supportive of the planned collaboration with Vuja De, beginning with Dr. Khanna joining the leadership team and soon leading to comparative oncology clinical trials that will develop effective treatments for both human and canine cancer patients,” said Ames Prentiss, CEO of Ethos Veterinary Health.

Dr. Chand Khanna

Dr. Khanna was the longtime Head of the NCI Pediatric Oncology Branch’s Tumor and Metastasis Biology Section, and the Founding Director of the Center for Cancer Research, Comparative Oncology Program. His research interests and responsibilities focused on the problem of cancer metastasis and the discovery of new options to treat patients with metastasis. Dr. Khanna has over 100 publications in the area of cancer biology and therapy. He is currently the Chief Science Officer of Ethos Veterinary Health and President of the non-profit incubator of scientific innovation, Ethos Discovery (501c.3.). In these roles Dr. Khanna seeks to improve outcomes for human and pet patients with complex medical problems through the development of novel therapeutics and diagnostics.

Dr. Lee Helman

Dr. Helman is Section Head of Basic and Translational Research within the Children’s Center for Cancer and Blood Diseases and Director of the Cancer and Blood Diseases Research Program of the Saban Research Institute of Children’s Hospital Los Angeles. He is also Professor of Pediatrics in the Keck School of Medicine of USC. Dr. Helman has been studying the biology and caring for pediatric patients with sarcomas for over thirty years. He has also trained many investigators in the field of pediatric sarcomas. One current area of active research at Children’s Hospital Los Angeles focuses on using full genomic classification of osteosarcoma tumors to improve therapy, as well as testing novel therapeutic drugs and drug combinations in patients with osteosarcoma. Dr. Helman received his medical degree from the University of Maryland School of Medicine magna cum laude in 1980 and was elected to Alpha Omega Alpha. He has served as scientific director for clinical research in the Center for Cancer Research at the NIH until 2016. He was elected to the American Society for Clinical Investigation and the American Association of Physicians and is a founding member and past president of the Connective Tissue Oncology Society. He is a past member of the Board of Governors of the Clinical Center at NIH. In addition to his many appointments with different organization, he has been appointed director of the Osteosarcoma Institute.

About Comparative Oncology

In the setting of cancer drug development, comparative oncology involves the inclusion of dogs with naturally occurring cancer in clinical trials, where novel or repurposed drugs are tested to answer questions that cannot be answered in conventional animal models of cancer or human clinical trials.

About Osteosarcoma

Osteosarcoma is an aggressive cancer of the bone in dogs and human patients and is the most common type of bone cancer in children and teens. Despite successful control of the primary tumor and follow-up chemotherapy, metastasis continues to be the most common cause of mortality for both species. The last 30 years have brought little improvement in survival outcomes for children with osteosarcoma, despite intensification of therapy. Due to lack of improved outcomes, new approaches to therapy are highly needed. Furthermore, if targeted therapeutics are found to prevent metastasis in this human cancer, a strong biological rationale would exist for the evaluation of such a therapy in other human cancers.

About Ethos Veterinary Health

Ethos is a veterinary health company with hospitals across the U.S. providing advanced medical care for pets. Our approach includes a focus on transformative science, continuous learning, growth for team members, and the development of collaborative relationships. For more information, visit ethosvet.com.

About Ethos Discovery

Ethos Discovery is a 501(c)3 non-profit incubator of scientific innovation that seeks to improve health outcomes in pets and humans with complex medical problems, including cancer. For more information, please visit ethosdiscovery.org

About Vuja De Sciences

Vuja De is a biotechnology startup dedicated to developing cancer metastasis treatments that prevent cancer progression and recurrence. Our initial focus is osteosarcoma. We utilize leading laboratory technologies for metastatic preclinical endpoints in combination with Comparative Oncology to de risk and inform product development and maximize likelihood for successful human oncology clinical trials. We are testing repurposed drugs that have previously been in human clinical trials, as well as novel preclinical drugs. For more information, please visit vujade-life.com.

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Altruista Health Integrates InterQual Connect™ Solution to Automate Pre-authorizations in GuidingCare


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As an Alliance Partner, Altruista can support its health plan members in strengthening payer-provider relationships — Nilo Mehrabian, Vice President of Product Management, Decision Support, Change Healthcare

Altruista Health, an innovative provider of care management technology solutions for health plans and provider organizations, today said it is joining forces with Change Healthcare as a Validated InterQual Alliance Partner to deliver dramatically streamlined utilization management (UM) for Altruista customers who rely on the GuidingCare® technology platform.

“We are pleased to support Altruista Health in offering its customers automated pre-authorizations within the InterQual Connect medical review service. This integration allows health plans to approve routine requests in real time and free up UM staff to focus on requests that require further medical review,” said Nilo Mehrabian, Vice President of Product Management, Decision Support, Change Healthcare. “As an Alliance Partner, Altruista can support its health plan customers in strengthening payer-provider relationships.”

GuidingCare has integrated the InterQual Connect medical review service into its UM module and connected it with GuidingCare’s module for provider access, driving easier, faster and more transparent prior authorizations in support of quality care. The exception-based design streamlines administrative workflow to reduce manual processes and redundant medical reviews. This integration will work with any version of GuidingCare.

“We have multiple Altruista customers already leveraging this capability within their current GuidingCare workflows,” said Craig Wigginton, Altruista Health Chief Technology Officer. “Health plans considering an upgrade to the InterQual Connect medical review service can rest assured that this integration has been tested and is in place.”

InterQual Connect is a flexible SaaS solution, integrated into payer and provider health information systems. It pairs with InterQual® Criteria, available as a web service, with proven and secure connectivity to fill the gap in current care management systems. This mutually beneficial connectivity and function supports value-based care and more resources available to caring for plan members.

About Altruista Health

Altruista Health delivers care management and population health management solutions that support value-based and person-centered care models. Our GuidingCare® technology platform integrates care management, care coordination and quality improvement programs through a suite of sophisticated yet easy-to-use web applications. GuidingCare is the largest and most widely adopted platform of its kind in the United States. Founded in 2007 and headquartered in the Washington, D.C. area, Altruista Health has grown into a recognized industry leader, and was named twice as one of the Top Population Health Management Companies to Know by Becker’s Healthcare. Health plans and healthcare providers use GuidingCare to transform their processes, reduce avoidable expenses and improve patient health outcomes. For more information, visit http://www.altruistahealth.com.

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Liberty IT Solutions Awarded $4M System Center Configuration Manager (SCCM) Operability Enhancement Services Task Order


Liberty IT Solutions LLC, which specializes in Health Information Technology, has been awarded a four-year (12-month Base Period plus three 12-month Option Periods) Task Order (TO) to enhance operability of the System Center Configuration Manager (SCCM) for the Department of Veterans Affairs (VA).

SCCM is the VA’s central patching tool for all updates to endpoints enterprise-wide. Continued SCCM system health is vital to VA’s ability to deliver up-to-date services across the country. Under this TO, Liberty, along with its partner ManTech International Corporation, will support the SCCM hardware/software and updates needed to maintain this system health. This also includes support for VA field offices to enable staff to efficiently troubleshoot problems and conduct maintenance activities.

Liberty CEO, Bill Greene, says of the win: “Enhancing the operability of the System Center Configuration Manager is an important task that Liberty is looking forward to working on with VA. We are excited to continue to modernize SCCM, in keeping with our commitment to the future of Health IT and a higher standard of service for Veterans.”

As the number of endpoints continues to rapidly expand and diversify, Liberty will also work to modernize the system, incorporating innovative technologies and project management approaches that will enhance cloud and mobile capabilities on SCCM. These efforts will ensure that SCCM can continue to support care for Veterans now and as their needs develop into the future.

About Liberty

Liberty IT Solutions delivers transformative services and support to multiple government agencies across a diverse portfolio of Health IT projects. Our team believes that lines of code can change lives and is driven to enable that to happen more often, more securely and more efficiently.

If you would like more information about this topic, please contact Liberty IT Solutions at 571.356.9627 or email at transformation@libertyits.com.

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Lifecycle Biotechnologies Releases 2020 Company Prospectus


2020 Lifecycle Prospectus

This prospectus embodies our passion for continued learning, and we loaded it with valuable information.

Lifecycle Biotechnologies announces the release of its 2020 prospectus. The Lifecycle prospectus features not just part numbers like what can be found in most catalogs, but rather, insightful information into Lifecycle’s business, it’s manufacturing facilities, the industries it supports, and that is all linked to the impact it has on the global life science industry. The goal? To provide an intelligence system – accurate, real-time data, distributed broadly and quickly, and presented in detail so that the reader can see and react to patterns in deciding for themselves what to do. The prospectus is an informational story not just about how Lifecycle makes an impact with each and every product and how it helps its customer to gain efficiencies, current and new alike, but to showcase the scientific advancements each market is achieving.

“We started this approach with our 2019 catalog, a first for our company, but wanted to amplify the usability and value of it as we enter a new decade,” said Aaron Schieving, Vice President, Sales and Marketing for Lifecycle Biotechnologies. “This prospectus embodies our passion for continued learning, and we loaded it with valuable information. I challenge you to go through it and not learn something new.”

A prospectus is a brochure or other document describing the major features, attractions, or services of a place, institution, or business to prospective patrons, clients, owners, or members. Lifecycle’s prospectus expands on this definition with the many third-party published articles, penned by the Lifecycle team it includes. For those new to Lifecycle, the prospectus welcomes you into its facilities and demonstrates the company’s commitment to truly making a difference. For those long-term partners of the company, the prospectus will allow you to experience the same personalized experience you are accustomed to, as well as allow you to learn about additional ways to expand your relationship and simplify your supply chain while working with the same company you have come to know and trust.

“We are excited to be able to share our prospectus. It is available for download on the homepage of our website (http://www.lifecyclebio.com). Simply scroll down and click the option to download,” said Schieving. “It will be well worth the few second it takes to get your copy. You can also e-mail us at info@lifecyclebio.com to get your copy.”

To learn more about Lifecycle Biotechnologies, the industries it serves, or to get your copy of the new 2020 prospectus, please contact Lifecycle Biotechnologies at info@lifecyclebio.com, 817.840.7855, or http://www.lifecyclebio.com.

Based in Ft. Worth, TX, Lifecycle Biotechnologies has served the life science industry for over 40 years. Lifecycle’s products are the beginning of the lifecycle of the lifesaving and life-enhancing medical products used globally today. As a leading life sciences tools and service supplier, Lifecycle fully understands the critical role its products play in many of the world’s leading pharmaceuticals, medical devices, biologics, diagnostics, cellular agriculture, cell- and tissue-based products, and many other medical products. While Lifecycle’s products aren’t used to diagnose, treat, or cure patients, without their contribution, none of this would be possible.

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Modernfold’s New PureView® Glass Wall Partition Line Maximizes Operability, Durability, Design Flexibility


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These glass partitions have been thought through down to the last detail.

Modernfold’s new PureView® Glass Wall System combines distinctive beauty with exceptionally easy, reliable operation. High-quality manufacturing from this trusted industry leader provides a robust solution for many architectural settings, including banks, offices, lobbies, interior storefronts, arena skyboxes and other commercial, institutional, and hospitality applications.

Every PureView® Glass Wall System includes double-brush top and bottom seals for draft management, foot-operated face and end panel interconnecting floor bolts for maximum convenience and security. Combinations of straight, angled or segmented configurations are available to fit a variety of space division needs.

In addition to the base clear anodized aluminum rail finish, designers may also select from three additional anodized aluminum finish options. Designers also have the option to select from more than 170 RAL powder coat colors, enabling custom rail color selections to meet any design need.

The premium PureView® Plus expression of the line features convertible panels for variable egress which can be placed anywhere in the panel run – and a clean profile wherever the convertible panel is situated. PureView® Plus also features a concealed door closer in the top panel rail maintaining the slim profile of the PureView® system. PureView also takes advantage of the preprogramming capabilities courtesy of Modernfold’s Smart Track™ suspension technology.

“These glass partitions have been thought through down to the last detail,” said Bryan Welch, Modernfold Managing Director. “PureView® panels can be separated from or connected to others effortlessly, safely and quickly. Backed by Modernfold’s expert service capabilities, these installations ensure many years of satisfaction.”

For more information on the new PureView® Glass Wall System and the many other beautiful and technically advanced Modernfold wall partition systems, please visit http://www.modernfold.com.

About Modernfold

For more than 95 years, Modernfold, Inc. has been the premier provider of products that enable optimal space utilization. Whether the primary requirement is acoustical control, versatile space management, energy savings, or daylighting, Modernfold’s innovative product solutions assist and facilitate building management. Beginning in 1925, the company helped invent the movable wall industry. Its current product line continues that leadership.

In a wide range of installations, outstanding, highly flexible results are provided by Modernfold Operable Partitions, Movable Glass Walls, Acoustically rated Acousti-Clear® Glass Wall systems, Acousti-Seal® Encore®, Acousti-Seal® Encore® Automated, Accordion Doors and ComfortDrive®.

About dormakaba Group

Modernfold became part of the dormakaba Group in 2015; Skyfold in 2017. dormakaba Group offers innovative, reliable access, security, and space division solutions in corporate environments, hotels, shops, sports facilities, airports, and much more. dormakaba is one of the top three companies of access control and security solutions on the global market as well as one of the leading global companies in the space division industry.

With strong brands in its portfolio, dormakaba and its numerous cooperation partners are represented in over 130 countries worldwide. The company has over 150 years of experience as a trusted partner for products, solutions and services for access to buildings and rooms from a single source. dormakaba is listed at the SIX Swiss exchange, is headquartered in Rümlang (Zurich/Switzerland) and generated a turnover of over CHF 2.8 billion with more than 16,000 employees in financial year 2017/18.

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CytomX Therapeutics Deploys Genedata Bioprocess


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Our decision to adopt the Genedata Bioprocess platform is based on its ability to directly integrate with our laboratory equipment and automate all data transfer, capture, processing, and data analysis and interpretation.

Genedata, the leading provider of enterprise software solutions for biopharmaceutical R&D, today announced that CytomX Therapeutics, a clinical-stage oncology-focused biopharmaceutical company, has licensed Genedata Bioprocess® to act as an integrated workflow backbone for its bioprocess development operations. CytomX will use Genedata Bioprocess to streamline and automate its process development workflows and to make the development of next-generation production processes more efficient.

“As our portfolio of novel drug candidates continues to rapidly expand, we needed to ramp up our development operations to keep pace. Genedata Bioprocess ensures the upscaling of our new drug manufacturing processes,” said Sridhar Viswanathan, Ph.D., Senior Vice President, Process Sciences and Manufacturing Operations at CytomX Therapeutics. “Our decision to adopt the Genedata Bioprocess platform is based on its ability to directly integrate with our laboratory equipment and automate all data transfer, capture, processing, and data analysis and interpretation. By enabling true high-throughput processes, we can significantly reduce time, effort, and costs within our daily operations.”

Genedata Bioprocess has been implemented in CytomX’s process development groups, with a focus on managing and interpreting bioreactor online and offline data. In particular, the platform will be used for CytomX’s novel class of antibody therapeutics based on its Probody™ therapeutic technology platform. Genedata Bioprocess will be used across all R&D programs at CytomX, including both proprietary and partnered R&D programs.

End-to-end (E2E) Workflow Platform for Bioprocess Development & CMC

Co-developed over the last six years with major biopharmaceutical companies, Genedata Bioprocess has been adopted by large, multinational biopharmaceutical companies and CMOs, as well as by smaller, innovative biotechnology organizations. The platform integrates all data generated along the biopharmaceutical development and CMC process, including upstream (USP), downstream (DSP), and analytics functions. It enables fully-automated processes, such as streamlining highly parallelized scale-down expression experiments in ambr® mini-bioreactors and data processing for large-scale bioreactors. In addition, by providing a central platform, it accelerates and improves the drug candidate’s transition from research to development. Built on a modular and scalable architecture, the platform is suitable for installations ranging from single-site groups to global, multi-site biopharma development organizations.

“We are delighted that CytomX, a leader with an innovative oncology drug development platform, has implemented Genedata Bioprocess to streamline their biopharma development operations,” said Othmar Pfannes, Ph.D., CEO of Genedata. “We are pleased to see that our integrated R&D workflow platform helps our rapidly growing customer base to reduce R&D process complexity, thereby enabling a cost-efficient development of innovative drugs that will help patients worldwide.”

About Genedata

Genedata transforms data into intelligence with innovative software solutions and domain-specific consulting services that automate complex, large-scale experimental processes and enable organizations to maximize the ROI in their R&D, spanning early discovery all the way to the clinic. Founded in 1997, Genedata is headquartered in Switzerland with additional offices in Germany, Japan, Singapore, the UK, and the US.

http://www.genedata.com

LinkedIn | Twitter | YouTube

________________________________________

Contact

Miles Fisher-Pollard

Genedata

Public Relations

Phone: +41 61 511 85 61

pr@genedata.com

Disclaimer

The statements in this press release that relate to future plans, events or performance are forward-looking statements that involve risks and uncertainties, including risks associated with uncertainties related to contract cancellations, developing risks, competitive factors, uncertainties pertaining to customer orders, demand for products and services, development of markets for the Company’s products and services. Readers are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date hereof. The Company undertakes no obligation to release publicly the result of any revisions to these forward-looking statements that may be made to reflect events or circumstances after the date hereof or to reflect the occurrence of unanticipated events.

All product and service names mentioned are the trademarks of their respective companies.

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HealthSherpa enrolls over 1 million Americans during Open Enrollment Period


With the close of the open enrollment period in the 38 states using the federal health insurance Marketplace, HealthSherpa announced its 2020 open enrollment results.

Between November 1st and December 17th, 2019, HealthSherpa enrolled 1.2 Million people in ACA coverage – a 143% increase over the prior Open Enrollment period. Over 31,000 of these enrollees were able to take advantage of the deadline extension granted by the Centers for Medicare and Medicaid Services. In total, HealthSherpa accounted for over 14% of ACA enrollments across the 38 Federal Marketplace states.

Most HealthSherpa consumers found coverage for $47/month or less, and 72% enrolled in silver plans, which offer comparable coverage to employer-sponsored health insurance. In aggregate, HealthSherpa has enrolled over 3 million Americans in on-exchange health insurance since 2014.

HealthSherpa is one of a handful of companies approved to use the Department of Health and Human Services’ innovative new Enhanced Direct Enrollment (EDE) technology, and was the first company granted approval on November 28th, 2018. In the 2020 Open Enrollment Period, HealthSherpa hosted the EDE platform for 37,000 insurance agents and over 15 insurance carriers.

EDE permits private companies to carry out all enrollment and related activities for on-exchange health coverage. HealthSherpa is approved for Phase 3, which allows HealthSherpa to process all applications, including those for rare tax circumstances, end-to-end on HealthSherpa.com.

“Continued strong enrollment year over year shows that consumers and issuers alike are deeply invested in the ACA Marketplace,” said HealthSherpa CEO George Kalogeropoulos. “Technologies like Enhanced Direct Enrollment are making it easier than ever for issuers, agents, employers, and other stakeholders to help Americans enroll in comprehensive coverage, and to help them manage that coverage throughout the year. We are proud to be at the forefront of ACA enrollment and to have the privilege of helping millions of Americans access the peace of mind that can only come with high-quality, ACA-compliant coverage.”

About HealthSherpa

HealthSherpa partners with large employers, insurers, as well as insurance agencies and agents to support consumers searching for, enrolling in and utilizing high quality, affordable health insurance coverage. HealthSherpa only sells ACA marketplace plans, which have built-in consumer protections, and since its founding in 2014, has enrolled over 3 million Americans in Affordable Care Act coverage. For more information, visit http://www.healthsherpa.com.

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NeoTract Designates Dr. Greg Griewe as UroLift® Center of Excellence


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“We are proud to name Dr. Greg Griewe as a UroLift Center of Excellence and provider of care for men with enlarged prostate symptoms using the UroLift System treatment,” said Dave Amerson

NeoTract, a wholly owned subsidiary of Teleflex Incorporated (NYSE:TFX) focused on addressing unmet needs in the field of urology, today announced that Greg Griewe, MD, Pinehurst Surgical in Pinehurst NC, has been designated as a UroLift® Center of Excellence. The designation recognizes that Dr. Griewe has achieved a high level of training and experience with the UroLift® System and demonstrated a commitment to exemplary care for men suffering from symptoms associated with Benign Prostatic Hyperplasia (BPH), also known as enlarged prostate.

Recommended for the treatment of BPH in both the American Urological Association and European Association of Urology clinical guidelines, the FDA-cleared Prostatic Urethral Lift procedure using the UroLift System is a proven, minimally invasive technology for treating lower urinary tract symptoms due to BPH. The UroLift permanent implants, delivered during a transurethral outpatient procedure, relieve prostate obstruction and open the urethra directly without cutting, heating, or removing prostate tissue.

The UroLift Center of Excellence program is designed to highlight urologists who are committed to educating their patients on BPH and the UroLift System as a treatment option and consistently seek to deliver excellent patient outcomes and experiences.

“We are proud to name Dr. Greg Griewe as a UroLift Center of Excellence and provider of care for men with enlarged prostate symptoms using the UroLift System treatment,” said Dave Amerson, president of the Teleflex Interventional Urology business unit. “The UroLift System is a safe and effective treatment that allows physicians to treat men in-office under local anesthesia, so they can experience lasting symptom relief within days after receiving treatment.”

Over 40 million men in the United States are affected by BPH, a condition that occurs when the prostate gland that surrounds the male urethra becomes enlarged with advancing age and begins to obstruct the urinary system. Symptoms of BPH often include interrupted sleep and urinary problems and can cause loss of productivity, depression and decreased quality of life.

Medication is often the first-line therapy for enlarged prostate, but relief can be inadequate and temporary. Side effects of medication treatment can include sexual dysfunction, dizziness and headaches, prompting many patients to quit using the drugs. For these patients, the classic alternative is surgery that cuts, heats or removes prostate tissue to open the blocked urethra. While current surgical options can be very effective in relieving symptoms, they can also leave patients with permanent side effects such as urinary incontinence, erectile dysfunction, and retrograde ejaculation.

About the UroLift® System

The FDA-cleared UroLift System is a proven, minimally invasive technology for treating lower urinary tract symptoms due to benign prostatic hyperplasia (BPH). The UroLift permanent implants, delivered during a minimally invasive transurethral outpatient procedure, relieve prostate obstruction and open the urethra directly without cutting, heating, or removing prostate tissue. Clinical data from a pivotal 206-patient randomized controlled study showed that patients with enlarged prostate receiving UroLift implants reported rapid and durable symptomatic and urinary flow rate improvement without compromising sexual function*1,2. Patients also experienced a significant improvement in quality of life. Over 100,000 men have been treated with the UroLift System in the U.S. Most common adverse events reported include hematuria, dysuria, micturition urgency, pelvic pain, and urge incontinence. Most symptoms were mild to moderate in severity and resolved within two to four weeks after the procedure. The Prostatic Urethral Lift procedure using the UroLift System is recommended for the treatment of BPH in both the American Urological Association and European Association of Urology clinical guidelines. The UroLift System is available in the U.S., Europe, Australia, Canada, Mexico and South Korea. Learn more at http://www.UroLift.com.

About NeoTract | Teleflex Interventional Urology

A wholly owned subsidiary of Teleflex Incorporated, the Interventional Urology Business Unit is dedicated to developing innovative, minimally invasive and clinically effective devices that address unmet needs in the field of urology. Our initial focus is on improving the standard of care for patients with BPH using the UroLift System, a minimally invasive permanent implant system that treats symptoms while preserving normal sexual function*1,2. Learn more at http://www.NeoTract.com.

About Teleflex Incorporated

Teleflex is a global provider of medical technologies designed to improve the health and quality of people’s lives. We apply purpose driven innovation – a relentless pursuit of identifying unmet clinical needs – to benefit patients and healthcare providers. Our portfolio is diverse, with solutions in the fields of vascular and interventional access, surgical, anesthesia, cardiac care, urology, emergency medicine and respiratory care. Teleflex employees worldwide are united in the understanding that what we do every day makes a difference. For more information, please visit http://www.teleflex.com.

Teleflex is the home of Arrow®, Deknatel®, Hudson RCI®, LMA®, Pilling®, Rusch®, UroLift® and Weck® – trusted brands united by a common sense of purpose

# # #

For Teleflex Incorporated:

Jake Elguicze, 610.948.2836

Treasurer and Vice President, Investor Relations

Media:

Nicole Osmer, 650.454.0504

nicole@healthandcommerce.com

*No instances of new, sustained erectile or ejaculatory dysfunction

1. Roehrborn, J Urology 2013 LIFT Study

2.McVary, J Sex Med 2016

MAC00968-01 Rev A

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LumaCare Formed and it Unveils the LumaCare Duo, a Breakthrough Therapeutic “Cold Laser” Device for Healthcare Professionals & Mature and/or Active Lifestyle Adults


“The reality is that over the past five decades thousands of peer-reviewed articles, studies and reports have been published about the efficacy of Cold Lasers as part of certain treatment regimens,” said Kevin Waller, COO and co-founder of LumaCare.

After 32 years in Stealth Mode, LumaCare™ emerged today to announce its formation and unveil its first product: The LumaCare Duo™.

The first public demonstrations of the LumaCare Duo will be given in the LumaCare booth (#44868) in the Sands Convention Center in Las Vegas, Nevada during CES 2020, the largest consumer electronics trade show and conference in the United States. Additionally, LumaCare will preview the LumaCare Duo from 7—10:30pm tonight to credentialed journalists, analysts, and influencers during the PEPCOM Digital Experience! press event at the Mirage Hotel Events Center on the Las Vegas Strip.

The LumaCare Duo is a handheld, wireless, and rechargeable “Cold Laser” device that features two rotating emitter heads, one each at opposite ends of jointed arms, to offer nearly 180 degrees of motion for delivering three different pulsating spectrums of therapeutic light to injured body parts. Each emitter head has a peak combined power output of 60 Watts from the 15 laser diodes and LEDs, specifically:


  • Four Infrared laser diodes at 905nm (nanometer wavelengths),
  • Six Infrared laser diodes at 808nm, and
  • Five visible Red LEDs at 670nm, for a total of 30 laser diodes/LEDs per LumaCare Duo system.

Because the patent pending LumaCare Duo features two articulating emitter heads affixed to the ends of two movable arms, users can manipulate the device to direct therapeutic laser light at injured tissue from two directions at the same time. Additionally, having two emitter heads also allows LumaCare Duo users to focus more Infrared and visible Red light over a wider area if needed. Users may also choose to implement only one emitter head if that is what the treatment protocol requires.

BACKGROUND INFO ON LUMACARE AND “COLD LASER” THERAPIES

LumaCare is the brainchild of National Laser Company, a 32-year-old company focused on the industrial, commercial and medical laser marketplace, a firm that has primarily worked behind the scenes as a private label and/or original equipment manufacturer (OEM) and service provider to other laser companies.

Given this foundation of over 30 years of laser industry experience and expertise, the executive team at LumaCare is very familiar with the role of Cold Lasers / Low-Level Laser Therapy (LLLT) as a treatment protocol for a wide variety of chronic and traumatic injuries.

“The reality is that over the past five decades thousands of peer-reviewed articles, studies and reports have been published about the efficacy of Cold Lasers as part of certain treatment regimens,” said Kevin Waller, COO and co-founder of LumaCare. “In fact, the very first inkling of the potential therapeutic benefits of LLLT came in 1967 when Endre Mester discovered that treatments of Cold Laser light regrew hair on mice.

“Studies in the ensuing 50-plus years have shown particular benefit from three wavelength bandwidths: from 650—675nm for surface/skin-level treatments, from 800—825nm for medium depth treatments, and from 900—925nm for deeper tissue/joint treatments. Since Dr. Mester’s finding, hundreds of thousands of Cold Laser systems have been used to improve blood flow, boost oxygenation, reduce inflammation and pain, and enhance cellular recovery for traumatic and chronic injuries.”

MORE LUMACARE DUO DETAILS, PRICING AND AVAILABILITY

The LumaCare Duo weighs 10.75 ounces, measures 4.75- x 5.63- x 2.75-inches (height x width x depth) when folded/closed and 3.25- x 11.50- x 2.75-in. when fully open, while the emitter heads measure 2.1- x 2.7- x 0.6-in. The range of motion of the LumaCare Duo is ~90 degrees per arm and ~135° per emitter head, with a total range of motion of ~180° when the device is fully open.

The LumaCare Duo is classified by the U.S. Food and Drug Administration as a Class 1 laser and is expected to have a suggested retail price of under $3,000.00 (US). However, the LumaCare Duo is currently in the latter stages of review by the FDA, with 510K Clearance anticipated by LumaCare in early 2020.

As a result, the LumaCare Duo is not available for purchase or resale at this time.

Nevertheless, fully functioning LumaCare Duo units are available now for evaluation purposes by healthcare professionals, credentialed journalists, and other qualified individuals and organizations.

For more information, please contact LumaCare at 801-924-8791 or via email at info@LumaCareLasers.com.

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LumaCare and LumaCareDuo are trademarks of LumaCare.

CONTACT:

David Politis, LumaCare’s VP of Marketing & Sales, 801-556-8184 (cell), dpolitis@LumaCareLasers.com

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Medphine Offers 2020 Special Discount On Medical Billing Services


Medphine, a leading provider of US healthcare revenue cycle management services, is excited to welcome the new decade with great zeal, and with a promise to help more and more providers in experiencing freedom from financial burden. Medphine is offering a flat 20% discount to its first-time service users, enrolling in January 2020.

Medphine has provided full-stack revenue cycle management, billing and coding services from last one decade. The services be it front desk support or specialty-specific billing, are all aligned with the continually evolving healthcare landscape and ever-advancing technologies. It has enhanced it portfolio furthermore by taking an extra leap in helping healthcare organizations capture extra income through Chronic Care Management Assistance program, Patient Recall Services, and much more.

When asked about what makes clients trust Medphine as their service partner, Reetu Singh, CEO of Medphine said, “Medphine goes beyond the realm of a traditional medical billing company and has developed a culture which promotes excellence in work, our team is hardworking which reflects in our deliverables. We have successfully recovered practices from the verge of bankruptcy by deploying our team that takes untiring measures to recover their billable and today they credit Medphine for enabling them to multiply their practice and start new locations. We are expanding our portfolio and are acquiring new skills to be able to help more and more organizations in anything related to Healthcare.”

Today billing companies like to work on their proprietary billing platforms which blindsides the provider and their staff as they are not able to see the real action on patient’s claims and have to rely on monthly reports which further complicates and doesn’t always depict the clear picture of the practices actual financial health.

Medphine think from provider’s perspective thus we purposefully work on almost all major billing platforms such as eClinicalworks, Epic, Kareo, Athenahealth, Chirofusion, AdvancedMD, GE Centricity, etc. We enjoy sharing our learning with our clients which fulfills our objective to ensure transparency, visibility, and improvement in the financial performance of healthcare facilities. This is why we want more of our prospective clients to benefit from our services, said Reetu.

Medphine invests its time and resources to learn the billing environment and understand the uniqueness of each client. That is what makes Medphine stand out as a pioneer service provider who specialize in crafting customized solution to each of its clients.

Healthcare facilities that are looking for an expert RCM service provider to make the switch, or to take control of their finances, can now benefit from Medphine’s holistic approach which is now at a 20% discount rate for clients enrolling in January 2020.

About Reetu Singh:

Reetu started her journey in the healthcare industry as a medical biller using eClinicalworks and has efficiently learned all the intricacies of the medical billing process. She aims at bringing disruption in the healthcare industry with transparency. With over a decade of experience in US Healthcare RCM and billing landscape, Reetu taking Medphine forwards plans to fight and provide simple solutions to various challenges the healthcare industry is facing right now, such as Surprise medical bills, lack of mobility of records and high cost to patients. Reetu’s passion for continuously delivering better output has made Medphine stand proud in the list of top 10 RCM companies, earning the label of one of the most promising and trustworthy companies to work with.

About Medphine.com :

Medphine is a provider of exhaustive billing, coding, and revenue cycle management services to healthcare organizations in the United States. With the aim to streamline the RCM, maximize revenue, and reduce the overhead cost, they employ certified and experienced billers and coders and deploy the latest in technology.

From front desk support, appointment reminder through specialty-specific billing, and coding to transcription services for medical practices and pharmacies, Medphine’s holistic services guarantee minimum probability of claim denial and maximum profitability. Medphine has a long proven record of dispensing dedicated RCM services for ensuring a higher return on investment.

Contact:

Medphine.com

124 Little Falls Rd #205

Fairfield, NJ 07004

USA

Phone: 732-419-2907

Website: https://www.medphine.com/

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