Category Archives: Health

What is new in the field of Health. Trending topics, and cutting edge research in the are of Health. Press Releases that give us updates on Health.

Kokomo Solutions, Inc. Announces COVID19Tracker™ Cloud Software FREE to Communities, Schools, Healthcare Systems and Workplaces


“We all have loved ones who we care immensely for. Advocating public safety is the very core of what Kokomo24/7® stands for. It’s our duty to provide communities with the means to deal with this issue head-on,” says Daniel J. Lee, CEO, and founder of Kokomo Solutions.

COVID19Tracker™ is a cloud-based safety solution in mobile apps and web portals with case management, communication, and collaboration features. Designed to help provide situational awareness, report, track, and manage Coronavirus cases within schools, communities, healthcare systems and workplaces across the nation, COVID19Tracker™ is comprised of 3 cloud solutions powered by commercially available software, Kokomo24/7® Safety Cloud™.

Kokomo24/7® Safety Cloud™ is a Software-as-a-Service product that ensures safe environments for schools, communities, and workplaces through an easy-to-use, intuitive set of safety applications designed to give communities, local governments, schools, and health administrators the proactive insight and capability to manage coronavirus cases.

At the heart of Kokomo24/7® Safety Cloud™ is a proprietary A.I. Engine that gives administrators analytical data to help determine the probability of reported cases for proactive intervention. Incident Management System (Kokomo24/7® – IMS) provides a proactive approach to respond to and recover from incidents in a repeatable methodology. With the Anonymous Reporting System (Kokomo24/7® – ARS), communities, students, parents, and employees can submit health and safety concerns from a mobile app or website portal. These reports will be triaged by an A.I.-based TruScore™ scoring system. The data in TruScore™ is designed to help manage false positives and more precisely identify at-risk individuals and incidents. Kokomo24/7® Emergency Operations Center (Kokomo24/7® – EOC) provides emergency operation centers and safety officials with instant situational awareness so emergencies are thoroughly coordinated and managed with informed decisions. Additionally, the Emergency Operations Center (EOC) module provides communications across schools, local governments and emergency responders, and full resource management (HR, EQ, and Financial).

“We all have loved ones who we care immensely for. Advocating public safety is the very core of what Kokomo24/7® stands for. It’s our duty to provide communities with the means to deal with this issue head-on,” says Daniel J. Lee, CEO, and founder of Kokomo Solutions. “Our goal is to expand our footprint in the public to help other communities across the country embrace the benefits of cloud technology for improved health and safety.”

COVID247.org provides a deeper dive into Kokomo Solutions’ reasons behind the importance of launching the COVID19Tracker™. With the ever-increasing numbers of the Coronavirus around the world and more medical crises like it to come in the future, regarding the limited resources within communities, schools, and workplaces, Kokomo Solutions sees the usefulness behind their technology. Our solutions can be implemented in a matter of a few days because our Kokomo24/7® Safety Cloud™ is a cloud-based and agile. No hardware, an intuitive user interface, and a seamless setup. That’s how Kokomo Solutions was able to launch COVID19Tracker™ as soon as it learned the first case of death from the virus in Washington state.

Kokomo Solutions has deployed the Kokomo24/7® Safety Cloud™ at the second-largest school district in America. This school district uses Kokomo24/7® Safety Cloud™ to provide their district resources, and entire communities with scalable safety solutions that offer security to compliance standards supported with the latest technologies built on the most reliable cloud provider, Amazon Web Services.

About Kokomo24/7®

With deep public safety experience, Kokomo Solutions, Inc. is the company behind a cloud-based safety platform that helps educators reduce unsafe student incidents to ensure higher quality learning environments? The Kokomo24/7® Safety Cloud™ platform consists of three modular and easy-to-deploy, intuitive safety solutions designed to help reduce disruptive and harmful events in communities and schools. Incident Management (IMS), Anonymous Reporting (ARS) and Emergency Operations Center (EOC) comprise the platform to bring to community and school district leaders unprecedented visibility to the safety and well-being of their citizens and students. For more information on Kokomo Solutions, please visit http://www.kokomo247.com.

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Keller Grover LLP is Investigating Walgreens Data Breach


According to a February 2020 letter sent to affected individuals, Walgreens became aware of a data breach involving the Walgreens mobile app personal secure messaging feature. According to the letter, an application error allowed certain personal messages from Walgreens that are stored in a database to be viewable by other customers using the Walgreen mobile app. The letter states that patient information that might have been viewed by other customers included patient names, prescription numbers and drug names, pharmacy locations, and shipping addresses, where applicable.

“Medical information is considered to be among the most personal and private of information under California law,” says Keller Grover LLP attorney Eric A. Grover. “For that reason, healthcare providers are required to give patients timely notice of data breaches and the negligent release and disclosure of medical information can, under certain circumstances, give rise to claims by affected individuals for money damages.”

Similar medical data breaches involving the failure to properly secure medical information have given rise to class action lawsuits. Recently, for example, St. Joseph Health Systems finalized a class action lawsuit settlement valued at over $30 million involving St. Joseph’s alleged failure to properly secure its network, allowing patient information to become publicly accessible on the internet.

If you have any information about the Walgreens data breach or are a California resident that has been affected by the data breach and have questions, contact Keller Grover’s attorneys at 888-535-5291 or by email at info@kellergrover.com. 

Keller Grover LLP is a leader in the field of medical information privacy litigation and has represented clients in numerous medical data breach class action cases, including lawsuits against St. Joseph Health Systems, Stanford Hospitals and Clinics, Health Net and 21st Century Oncology. Keller Grover will not charge you for reviewing your information and all information that you provide to Keller Grover in the process of seeking legal advice will be held strictly confidential. (Attorney Advertising)

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Rimidi Unveils New App to Accelerate Patient Screenings for COVID-19


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“With the app, we can help keep potentially infectious individuals from exposing other patients or staff in the healthcare system in waiting rooms, emergency rooms, or triage before they are identified and separated.”

Rimidi, a cloud-based software platform, today announced the launch of its patient-reported outcomes survey app to help limit the spread of COVID-19 in healthcare settings. Currently, the app is in expedited beta testing by select U.S. health systems operating in the regions at the greatest risk of Coronavirus outbreak. Rimidi anticipates general availability of the app before the end of March 2020.

“One of the greatest challenges in China and across other countries that faced early COVID-19 outbreaks has been hospital-based transmission,” said Lucienne Ide, MD, PhD, founder of Rimidi. “With the app, we can help keep potentially infectious individuals from exposing other patients or staff in the healthcare system in waiting rooms, emergency rooms, or triage before they are identified and separated.”

Combatting Coronavirus Spread via Advanced EHR-integrated Technology

Along with their text message appointment reminder, patients are sent a brief COVID-19 screening survey inquiring about current symptoms and recent travel. Integrated within the electronic health record (EHR), patient responses are easily captured and analyzed by clinical teams. The survey respondents demonstrating potential risk of COVID-19 exposure, in accordance with the latest CDC guidelines, are immediately notified with the appropriate next steps of care and treatment options, while the healthcare system is confidentially made aware of the at-risk patient.

Ultimately, the simplicity and accessibility of Rimidi’s screening app will help minimize the spread and impact of COVID-19 in healthcare settings by reducing the number of undiagnosed patients interacting with patients seeking standard care. It will also limit exposure of healthcare staff to potentially infectious patients in settings that are not adequately prepared.

Dr. Ide added, “The need for such a screening app was advocated for in a JAMA article following the Ebola outbreak in 2014. Today, the potential COVID-19 public health emergency reinforces the healthcare industry’s need for interoperability and stronger data-sharing rules to ease the flow of information, which enables rapid deployment of a single application across multiple EHR platforms.”

Rimidi remains in close coordination with the Centers for Disease Control and Prevention and will incorporate new evidence and its evolving guidance into the screening app as it emerges. This may include ongoing remote monitoring and self-reporting by patients in quarantine, among other features.

For more information and to be notified when the app is widely available for healthcare systems, please visit rimidi.com/covid19.

About Rimidi

Rimidi is a cloud-based software platform that enables personalized management of health conditions across populations. Created by doctors, Rimidi avoids the disconnect in connected care by combining patient-generated health data with clinical data from the EHR to drive patient-specific clinical insights and actions. The net effect is a better health system with optimized clinical workflows that enable better decisions, better relationships, better outcomes and ultimately a better healthcare system. For more information, visit rimidi.com and follow us on Facebook, Twitter and LinkedIn.

Media Contact:

Cortney Williams

ARPR, on behalf of Rimidi

cortney@arpr.com

855.300.8209

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LabRoots Announces Neuroscience 2020 Virtual Conference to Promote Research Worldwide and The NIH BRAIN Initiative


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LabRoots, the leading scientific social networking website offering premier, interactive virtual events and webinars, will be hosting approximately 15,000 neuroscience researchers, clinicians, and scientists from around the globe who are dedicated to understanding the brain and nervous system. The annual, free Neuroscience Virtual Event will capture emerging developments in Neuroscience and the impact brain research has on society, together with the latest innovations.

With nearly 70 speakers, including two stellar keynote deliveries, 15 on-demand discussions, and 13 panels, Neuroscience 2020 showcases an extremely comprehensive program supported by the organizing committee of renowned academia and industry experts, The NIH BRAIN team, and dedicated sponsors.

Featuring neural circuit and behavior dynamics, cell diversity, tool and technology development, advancing human neuroscience: basic to clinical projects, and neuroethics presented by early career scientists diverse in background, The NIH BRAIN Initiative session will preview “a multidisciplinary approach to neuroscience.” The agenda also highlights the scourge of neurodegenerative diseases and dementia, and behavioral and psychiatric disorders to expand on the all-encompassing theme of the conference – brain function in health and disease.

This year’s agenda commences with a keynote academia speaker, Dario Alessi, FRS FMedSci FRSE, Director, Professor of Signal Transduction at University of Dundee, describing the nuts and bolts of the LRRK2 signaling pathway and how it is linked to Parkinson’s Disease, and new approaches that could be exploited to better diagnose the disease. Following, Dr. Walter Koroshetz, Director of the National Institute of Neurological Disorders and Stroke who played a significant role in the revolution in acute stroke care in the US and the growth of the neurointensive care field, will deliver a keynote presentation on The BRAIN Initiative and its promise for new Neurotechnologies to more effectively diagnose and treat neuro/mental/substance abuse disorders.

The featured notable speakers cover many significant areas of Neuroscience including open science and data sharing for behavioral neuroscience, understanding the pitfalls and advantages of cognitive testing in mouse models of disease, deciphering the spreading of neuropathologies in neuronal circuits using a high capacity microfluidics platform, and learning about a protein that is a potential key player in neurodegeneration and aging, and much more.

“This year’s Brain Initiative track will showcase the power of combining diverse expertise and teamwork in tackling some of the most challenging areas of contemporary neuroscience research,” commented Karen K. David, Ph.D., Program Director, BRAIN Initiative. “We are excited to feature through LabRoots the breadth of expertise of our early-career scientists and representative collaborative projects that tackle the circuit basis of behavior, cell diversity, resource development, and human neuroscience. Through Labroots’ virtual environment, we are able to feature the team neuroscience approach that can often be difficult to showcase through usual channels including conferences.”

“Progressing at a remarkable pace, Neuroscience is one of the most exciting fields of biomedical research and our interactive forum continues to lead our mission in sharing cutting-edge science on a global front,” said Greg Cruikshank, Chief Executive Officer of LabRoots. “We look forward to deepening the knowledge through valuable discussions, as the research of the human brain continues to evolve.”

Produced on LabRoots’ robust platform, this online environment with exhibit and poster halls, and networking lounge allows attendees to connect seamlessly across all desktop and mobile devices. By participating in this event, Continuing Education credit (1 per presentation) can be earned for a maximum of 40 credits.

For more information or to register for the event, click here. Participants can follow the conversation online by using #LRneuro.

About LabRoots

LabRoots is the leading scientific social networking website, and primary source for scientific trending news and premier educational virtual events and webinars and more. Contributing to the advancement of science through content sharing capabilities, LabRoots is a powerful advocate in amplifying global networks and communities. Founded in 2008, LabRoots emphasizes digital innovation in scientific collaboration and learning. Offering more than articles and webcasts that go beyond the mundane and explore the latest discoveries in the world of science, LabRoots users can stay atop their field by gaining continuing education credits from a wide range of topics through their participation in the webinars and virtual events.

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Cell and Gene Therapies – Trends, Supply Chain Challenges and Solutions, Upcoming Webinar Hosted by Xtalks


Xtalks Life Science Webinars

The criticality and specialized handling needed for each shipment requires seamless execution of a vein-to-vein supply chain throughout the journey, and the manufacturers of these complex therapies must also consider the reliability, quality and cost effectiveness of any solution.

To control and direct the power of a patient’s immune system in order to fight disease is both ground-breaking as well as complicated. While the success of cell and gene therapy strives to become more mainstream and is increasingly the focus of researchers, the longer-term potential requires exploration. Researchers and manufacturers must translate the progress of cell and gene trials into broader programs targeting larger populations. Scalability and manufacturability are two challenges that the industry faces.

Nevertheless, before commercialization, cell and gene therapies encounter many other challenges as they progress towards their goal. The criticality and specialized handling needed for each shipment requires seamless execution of a vein-to-vein supply chain throughout the journey, and the manufacturers of these complex therapies must also consider the reliability, quality and cost effectiveness of any solution.

Join Darren Dasburg, Global Head of Cell Gene Services, Marken and Jeff Stone, Senior Director, Global Program Management, Marken in a live webinar on Thursday, March 19, 2020 at 9am EDT (1pm GMT).

For more information or to register for this event, visit Cell and Gene Therapies – Trends, Supply Chain Challenges and Solutions.

ABOUT XTALKS

Xtalks, powered by Honeycomb Worldwide Inc., is a leading provider of educational webinars to the global life science, food and medical device community. Every year thousands of industry practitioners (from life science, food and medical device companies, private & academic research institutions, healthcare centers, etc.) turn to Xtalks for access to quality content. Xtalks helps Life Science professionals stay current with industry developments, trends and regulations. Xtalks webinars also provide perspectives on key issues from top industry thought leaders and service providers.

ABOUT MARKEN

Marken is a wholly owned subsidiary of UPS. Marken is the only patient-centric supply chain organization 100% dedicated to the pharmaceutical and life sciences industries. Marken maintains the leading position for Direct to Patient and Home Health care services, biological sample shipments and offers a state-of-the-art GMP-compliant depot network and logistic hubs in 51 locations worldwide for clinical trial material storage and distribution. Marken’s more than 1,000 staff members manage 85,000 drug and biological shipments every month at all temperature ranges in more than 150 countries. Additional services such as biological kit production, ancillary material sourcing, storage and distribution, shipment lane verification and qualifications, as well as GDP, regulatory and compliance consultancy add to Marken’s unique position in the pharma and logistics industry. http://www.marken.com

To learn more about Xtalks, visit http://xtalks.com.

For information about hosting a webinar, visit http://xtalks.com/why-host-a-webinar/.

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SAFE Health Selected as Finalist for 2020 SXSW PITCH


Cellphone screenshots of the SAFE App

The SAFE App

“Our goal is to empower young people to respect and protect their sexual health. We created a tool to have the conversation about sexual health between partners, while also providing access to easy and affordable testing…our mission is to end the spread and stigma of STDs in our lifetime.”

SAFE Health, a digital healthcare company focused on sexual health, has been selected as a finalist for the 12th annual SXSW Pitch® (formerly SXSW Accelerator) for its debut product, The SAFE App, which lets potential partners verify each others sexual health status and provides the easiest and least expensive way to get tested.

SXSW Pitch is the marquee event of South by Southwest® (SXSW®) Conference & Festivals (March 13 – 22, 2020) Startups Track, where leading startups from around the world showcase some of the most impressive technology innovations to a panel of hand-picked judges and a live audience. Out of the 937 companies that applied to present at SXSW Pitch 2020, SAFE was selected as one of 5 finalists in the Health, Wearables & Wellbeing category.

The event will be held the first weekend of SXSW Conference & Festivals on the fourth floor of the Downtown Hilton Austin, Salon D/E. The event will then culminate with the 2020 SXSW Pitch Awards Ceremony on Sunday evening, March 15, where winning startups from each category and a Best in Show winner will be announced and honored. SAFE and fellow finalists in the Health, Wearables & Wellbeing category will present on March 15th.

“Our goal is to empower young people to respect and protect their sexual health,”said Lauren Weiniger, co-founder of SAFE. “We created a tool to make it easier, and a little less awkward, to have the conversation about sexual health between partners, while also providing access to easy and affordable testing. It’s not about blame or shame, our mission is to end the spread and stigma of STDs in our lifetime.”

According to the CDC, STD rates have reached an all-time high in the U.S. for the fifth year in a row. Dating apps and social networks have played a significant role as they have expanded dating pools, enabling STIs to spread rapidly through diverse populations. The HIPAA-compliant SAFE App is the first real-world, practical solution to addressing what the CDC now calls a “public health crisis.” The app lets people import their medical records from any provider, so they can show their status on their phone (and confirm the status of their partners). The app also lets users schedule affordable testing at 30,000 locations across the country.

“For over a decade, SXSW Pitch has played a pivotal role in…giving promising companies the resources they need to succeed when it matters most and providing high profile exposure,” said SXSW Pitch Event Producer Chris Valentine. “Of the 503 companies who have participated since the competition’s inception, over 75 percent have gone on to secure funding and 16 percent have been acquired.”

For more information about SXSW Pitch and to view the complete list of finalists, visit: https://www.sxsw.com/pitch.

About SAFE App

SAFE App lets people show their verified STD status on their phone, and provides the easiest and least expensive way to get tested and treated. Users can import their medical records for free from any provider, or book testing at over 30,000 locations. SAFE has partnerships with many of the leading players in healthcare, including Quest, Labcorp, and Mayo Clinic. More than an app, SAFE is a movement to end the spread and stigma of STDs in our lifetime.

Download SAFE App here: http://www.safeapp.me

Photo assets can be found here: https://goo.gl/6zs47h

About SXSW

SXSW dedicates itself to helping creative people achieve their goals. Founded in 1987 in Austin, Texas, SXSW is best known for its conference and festivals that celebrate the convergence of the interactive, film, and music industries. An essential destination for global professionals, the event features sessions, showcases, screenings, exhibitions, and a variety of networking opportunities. SXSW proves that the most unexpected discoveries happen when diverse topics and people come together. SXSW 2020 will take place March 13 – 22, 2020. For more information, please visit sxsw.com.

Media Contact:

Bridget Garwood

The SAFE App

301-305-6284

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Cytonus, the US-based Biotech Platform Company, gains a boost from Strategic Partnership with Europe-based Phoenestra


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Cytonus is thrilled to gain the benefit of Phoenestra’s scientific excellence, quality IP assets, as well as the top talent of their highly experienced executives, who have decades of biopharma industry experience and were instrumental in the past development of more than eleven biologics that are n

With numerous products in its pipeline, Cytonus Therapeutics Inc. today announced a strategic partnership agreement with Phoenestra GmbH to accelerate Cytonus’ existing products and to expand the companies’ intellectual property assets. Cytonus is a biotech company founded in San Diego, California. Phoenestra is a biotech company located in Austria.

Phoenestra has developed IP assets in connection with cell reprogramming as well as non-invasive sources for cell lines. The strategic partnership with Cytonus will expand both companies’ combined IP assets through co-development collaboration projects. As part of the strategic partnership, Phoenestra will also provide Cytonus new manufacturing capabilities, including a new production facility focused on operating in full compliance with Good Manufacturing Practices (GMP). Since its inception, Phoenestra has focused on an end-to-end approach to ensure both quality control and scalability, starting with the efficient sourcing of material from unique cell sources and producing finished GMP-certified products.

“We are honored to join forces with Cytonus,” commented Phoenestra CEO and Founder Klaus Graumann, PhD. “Phoenestra will work to complement and accelerate Cytonus’ game-changing Cargocyte™ biotechnologies.”

“Our co-development projects will create fertile ground for further expanding the combined IP assets and pipeline of products for Cytonus and Phoenestra,” commented Phoenestra CFO and Founder Otto Kanzler.

“Cytonus is thrilled to gain the benefit of Phoenestra’s scientific excellence, quality IP assets, as well as the top talent of their highly experienced executives, who have decades of biopharma industry experience and were instrumental in the past development of more than eleven biologics that are now commercial products,” commented Cytonus’ Founder and CEO Remo Moomiaie-Qajar, MD.

About Cytonus Therapeutics Inc.

Cytonus Therapeutics Inc. is a San Diego based biotech company that has developed a vast platform of proprietary immunotherapeutic products to treat a wide range of medical conditions including cancers, infectious diseases, inflammatory diseases and cognitive disorders, and to improve patient outcomes. Its proprietary Cargocyte™ technologies are next-generation biomolecular delivery devices which have numerous medical applications across unmet therapeutic areas. Cargocytes™ are engineered to safely transport a multiplicity of therapeutic payloads into difficult-to-reach targeted tissues, and can be programmed to deliver selective, potent, and controllable “off-the-shelf” therapies. Cytonus’ vast platform of therapeutics and vaccines has the potential to improve the health and lives of people with life-threatening conditions. For more information, we invite you to visit the Cytonus website at https://Cytonus.com. Please follow us on Cytonus on LinkedIn and on Twitter at: @CytonusTx.

Statements in this news release other than strictly historical facts, such as statements about Cytonus’ plans and strategies, new and existing products and technologies, anticipated clinical and regulatory pathways, and markets for its products, are forward-looking statements. The words “believe,” “expect,” “aim,” “anticipate,” “estimate,” “project,” and similar expressions identify forward-looking statements that speak only as of the date hereof. Such statements involve risks and uncertainties that could cause actual results to differ materially from anticipated results due to many factors, including regulatory and development risks. The company undertakes no obligation to publicly update or revise any forward-looking statement. This news release is neither an offer to sell, nor the solicitation of any offer to purchase, any security.

Join Cytonus on LinkedIn and follow its Twitter account at: @CytonusTx

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Crutchfield Dermatology Celebrates 2,000 Verified Positive Patient Reviews!


Charles E. Crutchfield III, M.D.

“I will never rush a patient who may face an unfavorable diagnosis. If I have to choose between compassion and keeping our schedule to the minute, we are going to run late.” – Charles E. Crutchfield III, M.D.

Whether replacing a furnace, installing new carpeting, or finding the best hotel for the next trip, chances are most people read online reviews to help make those selections. Online reviews are increasingly used to help find the best doctor, too. Studies show people benefit from learning about other people’s experiences.

“That’s why we are so proud Crutchfield Dermatology has received so many positive patient reviews,” says Charles E. Crutchfield III, MD, Medical Director of Crutchfield Dermatology. “Having over 2,000 people take the time to recount their positive experience at our clinic is one of the greatest honors we could receive.”

Dr. Crutchfield explains that, like any business, the clinic is “far from perfect.” But it’s the commitment to actively working on getting better every day that sets the clinic apart.

“When a review touches on an experience that is ‘less than ideal’ it gives us a chance to improve,” Crutchfield explains.

The emergence of online reviews as a prominent information source for consumers comes with challenges. Online reviews for physicians and other professional industries have an inherent selection bias.

For example, many negative reviews will express dissatisfaction that a medical condition isn’t cured when it’s well-known there is no cure for the disease. In those cases, which are not the fault or responsibility of the physician, there is no way to satisfy the patient.

Likewise, businesses can take the blame for third-party actors. For instance, a patient may feel a medicine costs too much or be upset that their insurance does not cover it. Even though this is beyond the control of the doctor, the patient will attribute the problem to that clinic rather than the health plan denying payment or pharmaceutical company charging the high price.

With over 2,000 verified, positive reviews about the quality of Crutchfield Dermatology’s services, are there any concerns expressed by patients about the clinic?

“Yes, of course,” responds Clinic Manager, Tim Quesnell. “Like all clinics, patients don’t like to wait.”

Whether it stems from sensitivity to the value of time in an increasingly fast-paced world, or some other cause, medical clinics and other service businesses struggle to maximize access to their services while minimizing wait times.

“We work every day to improve the schedule,” Quesnell says. “But medicine is not like the restaurant business. Things come up every clinic, and sometimes patients need extra attention.”

Crutchfield adds, “I will never rush a patient who may face an unfavorable diagnosis. If I have to choose between compassion and keeping our schedule to the minute, we are going to run late. Most people who have to wait when those conditions arise realize that if they were ever in need of a little extra attention, we would give it to them, too.”

But not all people look at commercial experiences with that level of empathy, which is why the 2K mark for positive reviews is so remarkable.

“Most people who have a great result or outcome go on with normal life. They go shopping with friends, run errands, and do other routine things that don’t include writing a review,” explains Darrin Rosha, a Minnesota attorney who works with clients on reputation issues. “People don’t usually run to their computer to express how happy they are. Rather, the desire to vent about a negative experience is far more powerful.”

Because so many patients have positively reviewed Crutchfield Dermatology, a remarkable occurrence in its own right, those reviews and word of mouth among professionals have resulted in over a thousand physicians sending patients Crutchfield Dermatology for dermatologic expertise and care. Although reviews and referrals reflect how Crutchfield Dermatology is a center of excellence and in high demand, there are aspects of the clinic that reviews don’t show.

For instance, many dermatology clinics pass more and more of their patient contact and care to mid-level personnel. Dr. Crutchfield has refused to hire physician assistants or other midlevel providers: He insists on seeing, diagnosing, and treating his patients personally. This commitment to patient care has resulted in the premium care Dr. Crutchfield is known for and fiercely proud of.

“We know we are in demand, and that leads to access challenges. We tell patients if they have a time-sensitive schedule that will not allow them to wait if necessary, we are probably not the right practice for them, Crutchfield continues.

Quesnell adds, “But if a patient demands the highest quality care and the knowledge that they will be seen by a professor of dermatology and one of the best board-certified dermatologists in the country, Crutchfield Dermatology welcomes them with open arms.”

It’s easy to see why Crutchfield Dermatology is so proud to have received over 2,000 verified, authentic positive patient reviews located at http://www.CrutchfieldDermatologyReviews.com

About Charles E. Crutchfield III, M.D.:

Charles E. Crutchfield III, M.D. is a graduate of the Mayo Clinic Medical School and a Clinical Professor of Dermatology at the University of Minnesota Medical School. He currently is the Medical Director of Crutchfield Dermatology in Eagan, (serving the greater Minneapolis-St. Paul area), Minnesota. Dr. Crutchfield is an annual selection of the “Top Doctors” issue of Mpls. St. Paul magazine. He is the only dermatologist to have been selected as a “Best Doctor for Women” by Minnesota Monthly magazine since the inception of the survey. Dr. Crutchfield has been selected as one of the “Best Doctors in America,” an honor awarded to only 4% of all practicing physicians. Dr. Crutchfield is the co-author of a children’s book on sun protection and dermatology textbook. He is a member of the AΩA National Medical Honor Society, an expert consultant for WebMD and CNN, and a recipient of the Karis Humanitarian Award from the Mayo Clinic School of Medicine. Dr. Crutchfield was also given “first a physician” award, Healthcare Hero, 100 most influential healthcare leaders in Minnesota, and one of the Top 100 African –American Newsmakers in the United States by TheGrio, an affiliate of NBC News. https://en.wikipedia.org/wiki/Grio_Awards

Vantage Consulting Group Paves Way for Drug Manufacturers to Implement and Demonstrate GS1 EPCIS 1.2 Compliance for FDA’s DSCSA Track and Trace Requirements


Drummond is pleased to announce that QU4RTET 3.0 has earned Drummond’s EPCIS 1.2 Certification seal. Vantage can now engage with their clients for implementation of QU4RTET so that these manufacturers can then earn their GS1 EPCIS 1.2 Trustmark’s for the Manufacturer Test Scenarios.

Drummond Group, the trusted leader in software compliance and interoperability testing, announced Vantage Consulting Group selected Drummond for the validation and certification of the Level-4 open source solution QU4RTET 3.0 in accordance to GS1 US Rx EPCIS Conformance Testing Program.

Drummond is pleased to announce that QU4RTET 3.0 has earned Drummond’s EPCIS 1.2 Certification seal. Vantage can now engage with their clients for implementation of QU4RTET so that these manufacturers can then earn their GS1 EPCIS 1.2 Trustmark’s for the Manufacturer Test Scenarios.

With GS1 US overseeing the program, Drummond validated QU4RTET’s compliance to all seven manufacturer role-based test scenarios as defined by GS1 EPCIS 1.2 Implementation Guidelines.

Vantage is taking a leadership role in ensuring EPCIS 1.2 messages between the manufacturer and the wholesaler are following the proper format and structure to support DSCSA track and trace requirements. Vantage recognizes the following advantages in bringing QU4RTET into compliance, the first L4 Software Solution to be validated and certified by Drummond for EPCIS 1.2.

  • It is essential to demonstrate compliance to the FDA’s Drug Supply Chain Security Act (DSCSA) for traceability in the supply chain
  • Earning the Drummond EPCIS 1.2 Certification seal is the first step in demonstrating compliance to DSCSA interoperability requirements for serialization. It is very important to us as a QU4RTET integration provider to ensure our customers can implement a GS1 EPCIS 1.2 certified solution so that they can earn their GS1 Trustmark for their implementation of QU4RTET 3.0

“Drummond’s rigorous yet intuitive EPCIS Conformance Portal, a web-based compliance testing service, was key to providing us with a straightforward way to demonstrate QU4RTET compliance to GS1 EPCIS 1.2 Implementation Guidelines. This provides assurance to our customers that Vantage is committed to guiding pharmaceutical manufacturers toward meeting DSCSA track and trace requirements” said George Poltorak, Vantage Consulting Group CEO.

“Drummond was the first testing service to be certified by GS1 and we are pleased to announce QU4RTET 3.0 has been conformance validated against GS1 EPCIS 1.2 Implementation Guidelines, which define how GS1 standards can be used to meet DSCSA track and trace requirements in an interoperable way” said Aaron Gomez, Drummond, Principal, Supply Chain Security business unit.

Further, Drummond is committed to the GS1 EPCIS Conformance Program and we welcome any stakeholder in the pharmaceutical supply chain impacted by FDA’s DSCSA mandate to contact Drummond to learn more about this testing service and for inquires to discuss how to gain trial access and a request demonstration.

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About Drummond

Drummond offers a comprehensive suite of services (including GS1 GDSN Data Pool Certification Testing), to help you achieve compliance with regulatory information security mandates and ensure critical business applications meet interoperability and application conformance. Increase trust, gain expertise and experience our proven methodologies and attention to detail as we partner with you for your long-term success. For more information visit: drummondgroup.com

About Vantage Consulting Group

Vantage is the manufacturing productivity company. For manufacturers facing safety, quality, or efficiency challenges, we provide strategic guidance and cost-effective execution of initiatives to improve serialization, packaging, inspection and more. Our team is seasoned, lean, on time and within your budget. vantage-cg.com.

About QU4RTET

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iaedp™ Symposium Shows Value of Collaboration in Decision Making in Eating Disorder Treatment


Collaboration between providers of various disciplines is a vital part of clinical practice in the treatment of eating disorders.

Collaboration between providers of various disciplines is a vital part of clinical practice in the treatment of eating disorders. Caring for complex patients at varying levels of treatment and in different environments requires that healthcare practitioners gain and practice effective interdisciplinary communication skills.

At the International Association of Eating Disorders Professionals (iaedp™) 2020 Symposium, the presentation “Difficult Cases: the Art and Science of Clinical Decision Making” will address all eating disorder treatment professionals to enhance their clinical decision making, case conceptualization and communication skills through intra- and interdisciplinary discussion.

During the session, presenters Michaela Voss, MD, Joanna Wiese, PhD and Isabelle Bouchard, MS, RD, LD will review cases that include transgender adolescents, chronic failure-to-thrive children, high-performing athletes, individuals with limited socioeconomic resources and multi-cultural families.

Dr. Voss, graduated medical school from University of Kansas Medical Center–Kansas City, KS, in 2010. She completed pediatric residency in 2013 at Children’s Hospital of Wisconsin – Milwaukee and graduated from adolescent medicine fellowship in 2016 at Seattle Children’s Hospital – Seattle. Dr. Voss joined the Adolescent Medicine Department at Children’s Mercy-Kansas City in 2016. Her current clinical focus includes eating disorders, transgender care, and mental health. Her research including eating disorders within the transgender community and creating a national eating disorder database with the Society of Adolescent Health and Medicine.

Dr. Wiese is a psychologist at Children’s Mercy Kansas City outpatient eating disorder specialty clinic and an Assistant Professor at the University of Missouri Kansas City Medical School in the department of Pediatrics. She has treated eating disorders in a variety of inpatient, residential and outpatient treatment settings and has done research on eating disorders and help seeking behaviors among college students. She also has clinical training and research experience in behavioral treatments for eating disorders, including family-based treatment.

Bouchard obtained her bachelor’s degree from Kansas State University and her Master’s in Dietetics and Nutrition from the University of Kansas. Her Master’s thesis focused on respiratory quotient as a metabolic indicator of health. Bouchard’s current clinical focus is in treating adolescents and adults with eating disorders and disordered eating. She is the owner of Bamboo Nutrition, an outpatient practice for eating disorders in Columbia, MO.

The 2020 iaedp™ Symposium is slated for March 26-29 at the Omni at ChampionsGate in Orlando. Registration and Exhibit Hall space are still open. For more information, visit iaedp.com.

About the iaedp™ Foundation: Since 1985, the International Association of Eating Disorders Professionals has provided education and training standards to an international and multidisciplinary group of various healthcare treatment providers and helping professions. MemberSHARE.iaedp.com is an iaedp™ business journal and online member resource to learn about noteworthy member achievements, continuing education webinars and U.S. and international chapter activity and events; for more information, visit MemberSHARE.

The Presidents Council provides iaedp™ support and includes: Center for Change; Center for Hope of the Sierras; Center for Discovery; Eating Recovery Center; Willow Place; Laureate Eating Disorders Program; McCallum Place Eating Disorder Centers; The Meadows Ranch; Rogers Behavioral Health; Rosewood Centers for Eating Disorders; Selah House; The Renfrew Center; Timberline Knolls; Veritas Collaborative; Alsana Eating Disorder Treatment & Recovery Centers; Silver Hill Hospital, Walden Behavioral Care and KIPU.

The 2020 iaedp™ Symposium is proud to announce Bronze Sponsors: ViaMar Health, Eating Disorder Recovery Specialists, Simple Practice, Transcend ED, Fairwinds Treatment Center and Montecatini.

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