All posts by imreal

National Counseling Practice Opens First Florida Office, Offers Extended Hours


Thriveworks, a counseling practice with 100+ locations across the US, has opened its first Florida office in Fort Lauderdale.

Thriveworks differentiates itself from other counseling practices by providing extended evening and weekend hours, offering flexible cancellations, and accepting most major insurance plans. Additionally, they offer online counseling opportunities.

Regional Clinic Director Ryan Culkin says, “We’re seeing that healthcare services fail to meet the scheduling needs of normal hardworking individuals and their families. We knew we could help change that—at least for mental health counseling.”

Thriveworks offers extended hours, from early morning to evening and weekend appointments. Normal hours of operation are 7:30am-9:00pm, Monday-Friday and 8:00am-5:00pm, Saturday-Sunday.

About Thriveworks:

Thriveworks is known for premium mental health services and customer care. On top of their extended hours, Thriveworks works to provide innovative technologies that supplement the therapy process including phone and email access to one’s therapist as well as a counselor-moderated community discussion board.

Thriveworks offers a variety of mental health services including individual therapy, couples therapy, life coaching, and help for specific issues like depression, anxiety, and addiction.

The Thriveworks philosophy is that everyone can benefit from working with a skilled caring therapist, counselor, or coach. For more information, call (754) 400-5514 or visit https://thriveworks.com/fort-lauderdale-counseling/

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Car Insurance Experts Present The Best Safe Driving Tips For Teen Drivers


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“Teen drivers should always keep their focus on the road and avoid any distractions. Also, they should never forget to wear the seatbelts”, said Russell Rabichev, Marketing Director of Internet Marketing Company.

Compare-autoinsurance.org has launched a new blog post that explains how safe driving teens can obtain better car insurance rates.

For more info and free quotes, please visit https://compare-autoinsurance.org/top-safe-driving-tips-for-teen-drivers/

Car insurance companies classify teen drivers as high-risk. The statistics show that teen drivers are more likely to be involved in car accidents, and for this reason, they will pay more on their insurance premiums. However, even teen drivers can find methods to lower their insurance rates.

Before hitting the road, teen drivers should follow the next safe driving tips:


  • Inspect the car before driving. Teen drivers should always ensure their cars are ready before hitting the road. It is recommended to check the gauge levels, adjust the mirrors, and make sure the headlights are working. Also, teen drivers should ensure they have enough gas in the tank.
  • Minimize distracted driving. Anything that distracts a teen driver is a threat to his safety. Teen drivers should avoid texting on the phone, eating, applying makeup, or other distractions.
  • Always wear seatbelts. Teens should always wear their seatbelts while driving. Studies have already shown that wearing the seatbelt can save the lives of the drivers and their passengers.
  • Do not exceed the speed limits. Even if they are in a hurry, teen drivers should always follow the speed limits. Drivers who are caught speeding will receive a hefty fine or even have their license suspended. Speeding is also one of the leading causes of car accidents where teen drivers lost their lives.
  • Avoid driving with other teenagers. Teen passengers can easily distract other teen drivers, so it’s advised to better drive alone than together with other teenagers.
  • Attend a defensive driving course. These driving courses are extremely beneficial for teen drivers. Teens will learn how to avoid distractions and they will improve their driving skills. Also, insurance companies will offer a discount to teen drivers that manage to graduate a defensive driving course.

For additional info, money-saving tips and free car insurance quotes, visit https://compare-autoinsurance.org/

Compare-autoinsurance.org is an online provider of life, home, health, and auto insurance quotes. This website is unique because it does not simply stick to one kind of insurance provider, but brings the clients the best deals from many different online insurance carriers. In this way, clients have access to offers from multiple carriers all in one place: this website. On this site, customers have access to quotes for insurance plans from various agencies, such as local or nationwide agencies, brand names insurance companies, etc.

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Suppliers Partnership for the Environment (SP) Elects 2020 Executive Committee with Toyota’s Kevin Butt as Chair


SP provides a leadership forum for companies like Toyota to work together with our fellow automakers, suppliers and government and NGO collaborators to advance leading environmental sustainability practices and programs across the automotive supply chain…

The Suppliers Partnership for the Environment (SP) – an association of global automakers and their suppliers working together to advance environmental sustainability through the automotive supply chain – has announced the election of its Executive Committee Officers for 2020.

Kevin M. Butt, Director, Environmental Sustainability, Toyota Motor North America, Inc. has been elected to serve as Chair of SP’s Executive Committee in 2020.

“SP provides a leadership forum for companies like Toyota to work together with our fellow automakers, suppliers and government and NGO collaborators to advance leading environmental sustainability practices and programs across the automotive supply chain, and it is an honor to be elected to serve as the Chair of SP’s Executive Committee in 2020” stated Kevin Butt.

“On behalf of the Executive Committee, I would also like to thank SP’s outgoing Chair Randy Leslie of Johnson Controls for his many years of dedicated service as both a founding member and past Chairman of the Committee. We sincerely appreciate Randy’s longtime leadership and dedication to the mission of this organization,” continued Kevin Butt.

The slate of SP Executive Committee Officers elected for 2020 includes:


  • Chair: Kevin Butt, Director, Environmental Sustainability, Toyota Motor North America, Inc.
  • Vice Chair: Russell Brynolf, CEO, FTS Technologies Inc.
  • Finance Chair: Jim Laney, Senior Manager, Environmental, Safety & Health, DENSO International America, Inc.
  • Membership Chair: Alissa Yakali, Sustainability Manager, Honda of America Manufacturing
  • Work Group Chair: Jack Nunes, Vice President, Global Environment, Health & Safety, Lear Corporation
  • At-Large: Greg Rose, Director, Environment, Health & Safety, FCA US LLC
  • At-Large: Andrew Hobbs, Director, Environmental Quality Office, Ford Motor Company
  • At-Large: Reeshemah Howard, Mission Leader / Sustainability Manager, General Motors

Steve Hellem, Executive Director of SP stated, “The SP membership has elected a remarkable group of environmental sustainability leaders to serve on the Executive Committee and we look forward to working together with them to continue to advance the automotive industry’s leadership on environmental sustainability issues”.

About SP

The Suppliers Partnership for the Environment (SP) is an association of automakers and their suppliers working in collaboration with the US EPA and other governmental entities to identify and implement creative projects and programs that will advance environmental sustainability while providing economic value to the automotive supply chain through strategic action and engagement. http://www.supplierspartnership.org/

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With Rapid Adoption of the Fillmaster Auto, FLAVORx Makes Major New Investment in Its Leadership Team


Pharmacies are increasingly using automation, like the Fillmaster Auto, to streamline basic dispensing tasks so their pharmacists can focus on consulting with patients and providing great customer care.

In response to several successful roll-outs of their new Fillmaster Auto dispensing technology, Maryland-based FLAVORx Inc. has announced the hiring of Kevin Campbell and Jerry Telson as Corporate Vice Presidents. Campbell and Telson will be responsible for delivering on the company’s pledge to help their pharmacy partners improve the patient experience, gain market share, drive efficiencies, and reduce costs, with the Fillmaster Auto as the catalyst.

“We are delighted to welcome Jerry and Kevin to the FLAVORx family at this important time for our company and for our pharmacy partners,” said Stuart R. Amos, President and CEO of FLAVORx. “Pharmacies are increasingly using automation, like the Fillmaster Auto, to streamline basic dispensing tasks so their pharmacists can focus on consulting with patients and providing great customer care. Adding Kevin and Jerry to our leadership team allows us to more effectively collaborate with pharmacy owners and operators who are committed to delivering a better pharmacy experience.”

Kevin Campbell has 42 years of experience in retail pharmacy and pharma. He most recently served as the Executive Director of Sales and Business Development at Azurity Pharmaceuticals, formerly CutisPharma, where he oversaw the expansion and utilization of the company’s FI℞ST® unit-of-use prescription compounding kits. Campbell’s areas of expertise include Quality Assurance, Supply Chain/Logistics, Sales/Marketing, Management, and Commercial Operations.

Jerry Telson is a seasoned retail pharmacy executive, having spent the past 39 years at Walgreens. While there, Telson held many leadership positions, both in the field and at the corporate level. His roles included Store Manager, District Manager, Corporate Director of Operation Administration, and most recently, Director of Pharmacy and Retail Operations, a role in which he was responsible for the P&L of over 100 retail pharmacies.

FLAVORx provides dispensing automation technology and medication flavoring systems to over 40,000 pharmacies in the U.S. Their products allow pharmacists to get more done in less time, while helping their pediatric patients be more adherent to the medications they must take. FLAVORx has been in business since 1995. Their products have been used to custom flavor over 150 million prescription medications.

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STRmix Will Be Used in San Antonio, Golden, and Tucson Forensic Labs


Forensic labs in San Antonio, TX, Golden, CO, and Tucson, AZ have announced they will begin using STRmix™ to resolve DNA profiles in criminal investigations.

Sophisticated forensic software that can be used to resolve mixed DNA profiles previously thought to be too complex to interpret, STRmix™ is being regularly used in 51 forensic labs throughout the U.S. Another 60 U.S. forensic labs are now in various stages of STRmix™ installation, validation, and training.

San Antonio’s Bexar County Criminal Investigation Laboratory provides the citizens of Bexar County with comprehensive, impartial, reliable scientific analysis of evidence by experts skilled in the latest technology in forensic science.

The Jefferson County Regional Crime Laboratory, based in Golden, CO, provides services to all law enforcement agencies within Jefferson County, including the Jefferson County Sheriff’s Office and the Arvada, Golden, Lakewood, and Wheat Ridge Police Departments. The lab also provides training in a variety of forensic disciplines to law enforcement agencies.

Finally, the Tucson (AZ) Police Department Crime Laboratory is part of the Forensics Division of the Investigative Services Bureau, providing the Tucson community with quality forensic science and service.

These labs join a national list of forensic labs using STRmix™ that now includes the FBI and the Federal Bureau of Alcohol, Tobacco, Firearms, and Explosives (ATF). Internationally, STRmix™ is being used by nearly two dozen forensic labs in Australia, New Zealand, England, Scotland, Ireland, Finland, Dubai, Denmark, Switzerland, and Canada.

Since its introduction in 2012, STRmix™ has been used to interpret DNA evidence in more than 120,000 cases around the world. It has also been used successfully in numerous U.S. court cases, including 28 successful admissibility hearings.

“Forensic labs increasingly are using STRmix™ because of its success in producing usable, admissible DNA evidence in a wide range of criminal cases,” says John Buckleton DSc, FRSNZ, Forensic Scientist at the New Zealand Institute of Environmental Science and Research (ESR) and one of the developers of STRmix™.

Dr. Buckleton notes that labs using STRmix™ are reporting an increase of interpretable DNA in gun cases from about 40% to more than 70%. STRmix™ is also producing a much better return on investment by delivering a significantly higher rate of interpretable results in sexual assault cases.

A new version of STRmix™, STRmix™ v2.7, was introduced in late 2019. STRmix™ v2.7 includes several new features in response to improvements recommended by forensic labs to better address the on-the-job needs they regularly encounter. DBLR™, an application used with STRmix™, was also introduced last year. DBLR™ allows users to undertake superfast database searches, visualize the value of their DNA mixture evidence, and carry out mixture to mixture matches.

For more information about STRmix™ visit http://www.strmix.com

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New Report Introduces Benchmarks on Clinical Trials Vendor Qualification Process


A new report from Tufts Center for the Study of Drug Development establishes benchmarks for the vendor qualification process, a critical element of clinical trial set up and execution. According to its November/December Impact Report, the process volume and complexity of the vendor qualification process creates delays in initiation in 7% of clinical trials for biopharma sponsors and 14% of trials for Contract Research Organizations.

The analysis, conducted in collaboration with The Avoca Group, was based on data provided by 76 small, medium, and large pharmaceutical companies engaged in global drug development.

Among the key study findings summarized in the November/December Tufts CSDD Impact Report were the following:

  • In 2018, global spending for vendor qualification and requalification is estimated to be $375M, with 25,000 qualifications and requalifications conducted.
  • Vendor qualification assessment costs have large disparities and variances between companies; there is a need to standardize and optimize the process.
  • There is significant variation across the service provider domains evaluated; a standardized approach would greatly improve the efficiency of evaluations.
  • A high percentage of assessments, especially those conducted by larger companies, include customized areas of inquiry, which create challenges to streamlining and standardizing the processes involved.
  • There is no identifiable competitive advantage held by any company based on the approaches to vendor qualification examined; an industry-wide or third-party system might benefit every organization.
  • Cycle times for vendor qualification are lengthy and growing; the average total cycle time from an RFI request to a signed contract is 19.0 weeks for single-service providers and 26 weeks for multi-service providers.


“Evaluating external service providers is a time-consuming process that must meet the unique demands of each R&D program and account for, among other factors, regulatory compliance, risk management, cost efficiency, information technology expertise, operating, and financial controls and oversight,” said Ken Getz, principal investigator and deputy director of Tufts CSDD. “The volume and complexity of assessments needed to qualify and requalify potential vendors is increasing, and the benchmarks from this new study identify opportunities for drug developers to more effectively and efficiently manage this process.”

“The development of our new Diligent® Qualification Platform aligns with the vision we share with our partners to bring optimal efficiency and effectiveness to the quality and compliance elements of the clinical development process. With Diligent’s intuitive technology and suite of quality assurance assessment and auditing services, sponsors and CROs can rapidly identify, evaluate, and select clinical service providers,” said Patricia Leuchten, Founder and CEO of The Avoca Group. “Diligent accelerates the prequalification of clinical service providers by leveraging powerful analytical technology and industry-leading standards from the Avoca Quality Consortium®. Clients have seen significant reductions in vendor qualification cycle times, in most cases from weeks to days, using the Diligent Platform.”

Tufts CSDD, based in Boston, conducts a wide range of in-depth analyses on pharmaceutical issues and hosts symposia, workshops, and public forums, and publishes Tufts CSDD Impact Reports, a bi-monthly newsletter providing analysis and insight into critical drug development issues.

About The Avoca Group

The Avoca Group is a life science consulting firm dedicated to improving quality and compliance in clinical trial execution. Since 2011, the Avoca Quality Consortium, a collaborative of over 100 pharma, biotech, CRO, and clinical service provider companies, has led the industry in developing practical solutions for improving quality and execution in clinical trials. Companies benefit from Avoca’s insightful research, deep subject matter expertise, industry-leading approaches, and technology. Avoca offers platforms and tailored solutions to help clinical research companies increase quality, ensure compliance, and improve efficiency so that medicines can reach patients faster.

About the Diligent Qualification Platform

The Diligent Qualification Platform is a groundbreaking cloud-based technology platform as a service (PaaS) that streamlines and simplifies provider selection and qualification. Diligent makes identifying, evaluating, and selecting clinical trial providers more efficient and less expensive and meets today’s rigorous quality and compliance standards. Built on The Avoca Group’s extensive industry standards for clinical service provider qualification, Diligent meets the demands of today’s changing clinical trial landscape.

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AIM to Participate at SMTA Rocky Mountain Expo & Tech Forum


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AIM Solder, a leading global manufacturer of solder assembly materials for the electronics industry, is pleased to announce their participation in the upcoming SMTA Rocky Mountain Expo and Tech Forum taking place on January 23, 2020 at Mile High Stadium in Denver, CO. AIM will highlight their NC273LT low temperature solder paste for bismuth bearing alloys, RX18 and CX18 no clean flux cored solder wire along with their full line of solder assembly materials.

AIM’s NC273LT low temperature solder paste provides assemblers another tool to meet the changing needs of an evolving PCB assembly market. With peak reflow temperatures below 170°C, NC273LT minimizes component and substrate warping, reduces thermal exposure and saves energy. NC273LT paste improves the wetting performance of bismuth alloys to RoHS compliant plating and surface finishes. NC273LT provides long stencil life, excellent transfer efficiencies and minimizes solder balling common to bismuth bearing alloys. When thermal exposure during the assembly process is a limitation, NC273LT is an excellent RoHS compliant replacement.

AIM’s RX18 and CX18 continue to achieve unprecedented customer acceptance. Engineered for automated/robotic selective soldering, RX18 promotes thermal transfer, fast wetting and reduces voids/skips. Additionally, RX18 extends solder iron tip life and leaves minimal flux residue. CX18 is an operator friendly, low odor/smoke formula, and speeds soldering performance leaving a clear, electrically safe residue that does not require removal. Further throughput and reliability gains can be realized when CX18 and RX18 are combined with AIM’s REL61™ and REL22™ alloys. REL22 improves product survival in extreme thermal exposure operating environments such as under-hood automotive, avionics/aerospace and LED lighting. REL61 is ideally suited for industries which require a cost effective alternative to SAC305 with no loss of processing performance or durability.

To discover all of AIM’s products and services, visit the company at the SMTA Rocky Mountain Expo and Tech Forum for more information and to speak with one of AIM’s knowledgeable staff members.

About AIM

Headquartered in Montreal, Canada, AIM Solder is a leading global manufacturer of assembly materials for the electronics industry with manufacturing, distribution and support facilities located throughout the world. AIM produces advanced solder products such as solder paste, liquid flux, cored wire, bar solder, epoxies, lead-free and halogen-free solder products, and specialty alloys such as indium and gold for a broad range of industries. A recipient of many prestigious SMT industry awards, AIM is strongly committed to innovative research and development of product and process improvement as well as providing customers with superior technical support, service and training. For more information about AIM, visit http://www.aimsolder.com.

Upcoming Events:

February 4-6, 2020 – IPC APEX Expo, San Diego Convention Center, San Diego, CA

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NutraScience Labs “Wraps Up” 6th Annual Holiday Season Fundraiser; Donates 7,948 Pounds of Goods to Island Harvest


Giving back to our local community and offering assistance to our fellow Long Islanders has been a long-standing practice of our organization.

NutraScience Labs, an award-winning provider of vitamin and supplement contract manufacturing services, announced that its staff collected 7,948 pounds of goods and non-perishable items for Long Island families in need during the holiday season.

The donated items, ranging from bottled water, canned food, and baby products, were picked up by Island Harvest, Long Island’s largest hunger-relief organization, and distributed across its vast network of 570 food pantries, soup kitchens, and other community outreach centers just before Christmas. This was the sixth consecutive year that NutraScience Labs had partnered with Island Harvest. Since 2014, NutraScience Labs’ employees have donated an estimated 13,000 pounds of items.

Founded in 1992 by Linda Breitstone, the mission of Island Harvest is to end hunger and reduce food waste on Long Island. According to its website, Island Harvest has served over 300,000 people and delivered 130 million pounds of food, supplementing 108 million meals.

“Giving back to our local community and offering assistance to our fellow Long Islanders has been a long-standing practice of our organization,” said company Vice President of Contract Manufacturing, Vincent Tricarico. “While more needs to be done at the local and national level to raise awareness about hunger, I’m proud of the difference our team made in the lives of so many people this holiday season.”

In addition to Island Harvest, NutraScience Labs has donated countless amounts of time and money over the years to other charitable organizations, including the Make-A-Wish Foundation of Suffolk County, Wounded Warrior Project, and Vitamin Angels.

For further information, contact Vice President of Digital Marketing, Andrew M. Goldman at (855) 492-7388 or agoldman@nutrasciencelabs.com.

About NutraScience Labs, Inc.

NutraScience Labs, Inc., a subsidiary of Twinlab Consolidated Holdings, Inc., is an award-winning supplier of nutraceutical contract manufacturing services. Headquartered in Farmingdale, New York, the firm boasts more than 50 years’ of experience and has provided over 1,200 brands with best-in-class contract manufacturing, packaging, labeling, and fulfillment services. It has a long-standing reputation of excellence due to its ability to consistently deliver dedicated account management services, competitive price quotes, and rapid product lead times. For more information, visit NutraScienceLabs.com or call (855) 492-7388 to speak with a company representative.

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Cardea Bio Seeks to Accelerate Corporate Vision, Adds 3 Seasoned Executives to Senior Leadership Team


“We are thrilled to bring these exceptional people onboard to realize our vision of helping the world Conduct Biology™,” Says CEO, Michael Heltzen

Cardea Bio, a new (bio)technology infrastructure company pioneering the development of biology-gated transistors to integrate biology and electronics, announced today that it has added four highly successful and experienced leaders to its senior management team.


  • Dr. Paul Grint as Chairman of Innovation Council
  • Jonathan Seaton as Senior Vice President, Corporate & Business Development
  • Rob Lozuk as Senior Vice President, Commercial Operations

With decades of combined experience ranging from Paul Grint’s time as the former CEO of AmpliPhi and an Illumina Board member, Jonathan Seaton, Illumina’s former Senior Vice President (SVP) of Corporate & Business Development, after VP positions at BD Life Sciences and Roche, and Rob Lozuk’s executive positions at Sequenom and Thermo Fisher Scientific, Cardea has just positioned itself for accelerated growth under an experienced leadership team.

“This talent infusion enables Cardea to accelerate our business while validating the attractiveness of our vision and the substantial opportunity in front of us. We are thrilled to bring these exceptional people onboard to realize our vision of helping the world Conduct Biology™,” says CEO, Michael Heltzen.

Cardea has appointed Paul Grint, MD as its Chairman of the inaugural Cardea Innovation Council. In this position, Dr. Grint will lead a group of high-profile Innovation advisors and experts, who will be announced later in Q1 2020. Dr. Grint is a proven biotechnology executive with more than two decades of experience leading both established and emerging biotech companies working in the areas of infectious disease, immunology, and oncology.

Most recently, Dr. Grint was CEO and a member of the board of directors of AmpliPhi Biosciences, which recently merged with C3J Therapeutics to form Armata Pharmaceuticals. Dr. Grint has also served in senior management roles at Cerexa, Forest Laboratories, Kalypsys, Pfizer, IDEC Pharmaceuticals, and Schering-Plough Corporation.

“Cardea has created an entirely new way for scientists from any industry to access biology. The Innovation Council will leverage our members’ diverse technology and industry backgrounds from life sciences, bioinformatics, agriculture, electronics, diagnostics as well as food and environmental safety to identify innovation partners and new solutions to industry bottlenecks and problems,” said Dr. Grint.

Cardea’s Innovation Council is actively engaged in supporting the company’s mission to connect the domain of biology to more traditional technology and computer infrastructures, enabling greater access to bio-data in numerous applications; now referred to as the “Internet of Biology”.

Jonathan Seaton has joined Cardea as SVP for Corporate & Business Development where Mr. Seaton’s access to peers in the global life science world will be the starting point for more product co-development partnerships. Cardea’s biology-based transistor infrastructure will offer partner’s the tech modules to create a new generation of life science applications and devices branded and sold under the partner’s brand.

Prior to joining Cardea, Mr. Seaton held the position of SVP, Corporate & Business Development at Illumina, and prior to that he was VP, Strategy and Business Development at BD Life Sciences and Vice Director, Global Business Development at Roche Diagnostics.

“Cardea is pioneering a new method of life science detection and expanding the scope of possible insights. The Cardean infrastructure is not just generating data-sets, but also the data-streams of interactive signals from systems biology. It even allows for multi-omics analysis due to the biocompatible graphene transistors, which do not require the amplification and optics that often are the bottlenecks in life sciences,” says Mr. Seaton.

Rob Lozuk has been assisting Cardea throughout most of 2019 as an executive business consultant. Rob was initially responsible for building the Cardea Innovation Partnership Program and is now transitioning into a broader role as Cardea’s SVP of Commercial Operations, a role he also held previously at Sequenom, where he was responsible for sales, marketing, commercial and laboratory operations.

“Through our Innovation Partnership Program, Cardea is working with a select group of prestigious partners to create a new generation of “Internet of Biology” enabled products. Cardea’s proprietary, biology-gated transistor infrastructure will have an enormous impact on the world as partners will now be able to market new “biology is technology” applications inside instruments and/or portable devices only once imagined,” says Mr. Lozuk.

“It’s rare to have a detection breakthrough that significantly expands the number and type of applications within and outside of the traditional life science markets. Cardea’s technology leverages all of the learnings and methods of scaling from the well-established semiconductor industry while opening a whole new playing field in-between biology and electronics that has the capability of bringing valuable insights to every human being on the planet,” continues Mr. Lozuk.

About Cardea Bio

Cardea Bio is developing a new generation of (bio)technology infrastructure based on proprietary biology-gated transistors (“Cardean transistors”). Cardean transistors leverage biocompatible graphene instead of silicon and replace optical signal observations with direct electrical molecular signal analysis. Until now, life science data was comprised of static snapshot datasets. With Cardean transistors, the company and its Innovation Partners can generate streaming multi-omics data to measure real-time biological signals. Cardea is now manufacturing chips at scale and partners have started to significantly expand the amount, type and quality of biological data they capture by building products that Conduct Biology™. Cardea is headquartered in San Diego, California.

For more information, please visit cardeabio.com and engage with us on Twitter @Cardeabio or on LinkedIn.

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EnSoftek’s DrCloudEHR™ simplifies Patient Enrollment with its best practices module, Inbound Referral Management (IRM)


Inbound Referral Management (IRM) Module

As we start a new year and decade, EnSoftek continues to lead EHR systems with strong product development investments and is committed to enabling the highest levels of care through its DrCloudEHR suit of best practice solutions” said Ramana Reddy, CEO EnSoftek, Inc.

In yet another release to help its Customers become more efficient and minimize manual data entry tasks, EnSoftek announces the release of its latest “best practice module” for the DrCloudEHR solution, Inbound Referral Management (IRM). The DrCloudEHR IRM module offers an integrated, on-line data capture webpage for use by referral sources to send all of the necessary information with attached files in a simple, secure manner. A fast and easy to use solution requiring no training for referral sources and minimal training of agency intake staff, this module facilitates the entry of complete referral information into the EHR for evaluation and acceptance of the consumer.

As healthcare continues to shift focus towards “Value Based Reimbursement”, organizations need its staff to spend less time on administrative tasks and more time focused on the consumers. To do so, they need the right tools. The DrCloudEHR IRM module is exactly that. It helps eliminate redundant data entry and multiple phone, email and faxes to track down information. Behavioral Health and Human Services organizations are able to help more consumers and increase revenue by automating their referral process.

Utilizing DrCloudEHR, referring persons complete a Referral Form directly on the behavioral health organization’s web site. The submitted referral detail is automatically routed into DrCloudEHR for evaluation with all of the relevant information.

“As we start a new year and decade, EnSoftek continues to lead EHR systems with strong product development investments and is committed to enabling the highest levels of care through its DrCloudEHR solution for Behavioral Health and Human Services organizations. As a result of our continued efforts in listening closely to the needs of our partners, we consistently seek to develop easy to use best practice solutions that are the right fit for our Customers,” said Ramana Reddy, President/CEO of EnSoftek.

About DrCloudEHR™ and EnSoftek, Inc.

Currently in use in 26 states throughout the country, DrCloudEHR from EnSoftek is a meaningful use stage 3 certified (supporting Interoperability), native cloud electronic health records (EHR) system designed for behavioral health and human services organizations. DrCloudEHR, available with anytime, anywhere access, helps our customers deliver better services, improve patient care, engagement, health outcomes; and provide better overall patient satisfaction – making it the preferred solution for current and future behavioral health, health and human services, and integrated care providers.

EnSoftek, Inc. provides diversified enterprise IT solutions to both public and private sector enterprises.

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http://www.drcloudehr.com; http://www.ensoftek.com

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