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AgileBio Launches a LIMS Package Addressed to COVID-19 Labs

AgileBio Launches a LIMS Package Addressed to COVID-19 Labs

LabCollector LIMS developed by AgileBio is ready to join hands with the testing labs to increase the rapidity and efficiency of COVID-19 tests and its management thereby helping to eradicate the COVID-19 global pandemic.

To address that effort, AgileBio is offering a COVID LIMS pack withย  its main software LabCollector + LSM (Lab Service Management) + I-Collector automation + 2D rack scanner connectivity to any COVID-19 testing facility with free hosting for one year.

โ€œThe WHO recommendation is for massive Covid-19 tests everywhere and every day. The world is pressing tests and samples arrive by increasing batches. With LabCollector we help labs get organized and track samples and work. It was natural for us to propose our experience and tools quickly and without the burden of costs.โ€- Pierre Rodrigues, CEO & Founder of AgileBio, says.

The LabCollector COVID-19 pack is a mix of software components and all the needed service to bring labs online quickly. It also includes free online hosting for one year for LabCollector. Labs can now manage the COVID-19 samples from reception to result reporting, inventory for reagents & supplies, biobanking of COVID-19 samples with 2D Rack Scanners and much more with COVID-19 LC + LSM pack. This will increase the efficiency of labs by managing the tests request and speed with automation. A remote LSM portal application which is included in the pack will help the labs connect with unlimited number of doctors or providers of COVID-19 samples. It will also assist in communication of test updates, reports and invoices between the labs and the doctors/providers. All in all, the AgileBio offers all needed parts for test management to the labs and free consulting and quick setup and 1-year free web hosting (compliant with FDA) at an extremely reduced cost.

LabCollector by AgileBio also offers an extensive and modular tool set. It easily connects to 2D rack scanners to catalog samples from any scanner on the market. To automate test execution, AgileBio proposes a middleware I-Collector which allows quick integration of PCR/qPCR machines to help get the results transferred to LabCollector LIMS (into the Lab Service Management add-on) and ultimately to automatic positive/negative assessment and reporting.

Furthermore, AgileBio teams is also familiar with regulatory requirements a test lab needs and keeping this in mind we have included our compliancy pack in the COVID LC + LSM Pack. AgileBio team shall provide testing labs with first hand training and technical support to make implementation of LabCollector smooth and easy in your lab. Our trusted advisors and software integration experts will make your transition to LabCollector effortless.

About AgileBio

AgileBio, founded in 2002, is a leader in providing collaborative tools that enhance research productivity and traceability to scientist teams in industry and academia. ย AgileBioโ€™s mission is to develop flexible and innovative software, such as our main product,ย LabCollector, and thus, turn research teams into more agile structures.ย LabCollectorย is a unique Intranet based software, allowing centralized management of all your lab data. By usingย LabCollector, lab teams can benefit from efficient information sharing and access. ย AgileBio also builds and implements customized and packaged IT solutions that meet the demand of highly competitive companies and labs. Our clients turn to us time and time again because they trust us to get things right from the start.

Xerox and Vortran Medical Partnering to Mass Produce Disposable Ventilators

Xerox and Vortran Medical Partnering to Mass Produce Disposable Ventilators

Xerox Holdings Corporation and Vortran Medical Technology are teaming up to speed and scale production of Vortranโ€™s GO2Vent ventilator and related Airway Pressure Monitor (APM-Plus) for hospitals and emergency response units fighting the battle against COVID-19.

The two companies expect to work together to quickly respond to the shortage of critical ventilation equipment necessary to support patients breathing. Assuming a stable supply of essential parts, the companies will be rapidly scaling up production from approximately 40,000 ventilators in April to between 150,000 and 200,000 ventilators a month by June. Together, Xerox and Vortran could produce as many as 1 million ventilators in the coming months.

While the GO2Vent is not a replacement for ventilators found in intensive care units (ICUs), it is widely used in emergency situations, inter-hospital transport and MRIs. Given the shortage of ICU-grade ventilators, medical professionals are utilizing tools like this and other technology to support patients who do not yet or no longer need an ICU-level breathing device, which can be freed up for another patient.

โ€œOur smartest minds met (virtually) with Vortranโ€™s smartest minds and figured out how to mass produce this critical technology,โ€ said John Visentin, vice chairman and chief executive officer, Xerox. โ€œWe want to help make sure doctors, nurses and paramedics on the frontlines have the resources they need to help the rising number of patients with COVID-19.โ€

Xerox plans to manufacture these FDA-approved ventilators and APM-Plus devices at its facility outside of Rochester, NY, where the company was founded and maintains a large presence. Vortran will continue to manufacture ventilators at its current facility in Sacramento, CA.

โ€œThe partnership with Xerox has one clear goal โ€“ to help save as many lives as possible. With Vortranโ€™s proven technology and Xeroxโ€™s ability to hyper-scale manufacturing, we believe we can supply healthcare providers as many as 1 million ventilators in the coming months,โ€ said Vortran Co-founder and CEO, Gordon A. Wong, M.D. โ€œFor all of us, this will be the most important thing we ever do.โ€

Vortranโ€™s GO2Vent was designed for emergency use, natural disasters and disease outbreaks such as the COVID-19 pandemic. A gas-operated, disposable ventilator that can be set-up within minutes and discarded after use by a single patient, it provides support via a secure airway and can be operated on a compressor, oxygen or air with a minimum of 10 liters per minute flow rates.

The GO2Vent can provide continuous ventilatory support for up to 30 days and operates independent of Vortranโ€™s APM-Plus. The APM-Plus is a battery operated, portable device that connects to a GO2Vent and provides enhanced monitoring of patient status and key respiratory parameters. Given the need to confirm key supplies, the companies are actively assessing how quickly production can ramp for the APM-Plus devices.

In addition to scaling up production of the GO2Vent and APM-Plus, Xerox and Vortran expect to compile and analyze data and feedback from healthcare professionals on the frontlines of the battle against COVID-19 in order to design and mass produce external, in-line modifications that can be added to the GO2Vent to expand the potential applications of this life-saving equipment.

Both Xerox and Vortran will distribute the products.

About Xerox
Xerox Holdings Corporation makes every day work better. We are a workplace technology company building and integrating software and hardware for enterprises large and small. As customers seek to manage information across digital and physical platforms, Xerox delivers a seamless, secure and sustainable experience. Whether inventing the copier, Ethernet, the laser printer or more, Xerox has long defined the modern work experience. Learn how that innovation continues at xerox.com.

About Vortran
VORTRAN Medical Technology has been providing medical device excellence since 1983. We are a research, development, and manufacturing company of advanced medical respiratory and ambulatory devices. We serve domestic and international markets with a superior line of products for hospitals, emergency medical services (EMS), disaster preparedness, and MRI/CT applications in hospitals, acute care, post acute, homecare and EMS situations.

Co-Diagnostics, Inc Receives FDA Emergency Use Authorization for COVID-19 Test

Co-Diagnostics, Inc Receives FDA Emergency Use Authorization for COVID-19 Test

Co-Diagnostics, Inc. , a molecular diagnostics company with a unique, patented platform for the development of diagnostic tests, announced that its Logix Smartโ„ข Coronavirus COVID-19 Test has obtained Emergency Use Authorization (EUA) by the FDA to be used for the diagnosis of SARS-CoV-2. The Companyโ€™s test can be used by clinical laboratories certified under Clinical Laboratory Improvement Amendments (CLIA) to detect the presence of the virus that causes COVID-19, and is available for purchase from the Companyโ€™s Utah-based ISO-13485:2016 certified facility.

Co-Diagnostics began offering its COVID-19 test to some U.S. CLIA labs in March 2020 as a result of the FDAโ€™s policy for diagnostic tests for COVID-19 during the current public health emergency. Previously, the Company had initiated sales of its CE-IVD test to the European Community, and to other global markets that accept a CE marking as valid regulatory approval following routine local product registration.

CEO of Co-Diagnostics Dwight Egan commented, โ€œWe believe that this authorization confirms the quality and performance of our COVID-19 test, and that it is a significant step in opening more doors and helping this test to reach an even wider audience. Many experts agree that accessibility of widespread testing is an important element to โ€˜flattening the curveโ€™ as U.S. cases of COVID-19 continue to rise, and that increased testing throughput is vital to achieve this objective. We look forward to continuing our goal of increasing the availability of advanced, high-throughput, and cost-effective COVID-19 testing solutions both close to home and across the globe.โ€

The Co-Diagnostics Logix Smartโ„ข Coronavirus COVID-19 Test uses the Companyโ€™s patented CoPrimerโ„ข technology to target the RdRp gene of the SARS-CoV-2 virus. The advanced nature of CoPrimers has allowed Co-Diagnostics to design a highly-specific, single-well PCR test, allowing higher throughput over tests that require multiple wells. Co-Diagnostics believes the lower cost of reagents in the Companyโ€™s single-well test will help hospitals and laboratories to process more while paying less, benefiting healthcare providers and patients alike.

About Co-Diagnostics, Inc.:

Co-Diagnostics, Inc., a Utah corporation, is a molecular diagnostics company that develops, manufactures and markets a new, state-of-the-art diagnostics technology. The Companyโ€™s technology is utilized for tests that are designed using the detection and/or analysis of nucleic acid molecules (DNA or RNA). The Company also uses its proprietary technology to design specific tests to locate genetic markers for use in industries other than infectious disease and license the use of those tests to specific customers.

Synergy Laboratories Adds Medical Testing Expertise to Fight the Coronavirus and COVID-19

Synergy Laboratories Adds Medical Testing Expertise to Fight the Coronavirus and COVID-19

Synergy Laboratories (Synergy) adds its significant medical testing expertise to the fight against the coronavirus and COVID-19. Synergy began offering coronavirus testing to healthcare facilities on Wednesday April 1, 2020. Synergy is the first medical laboratory in South Alabama to offer these tests.

โ€œFast, accurate testing is one of the keys to combatting the spread of the coronavirus. Our new testing capability has been approved by the U. S. FDA and will dramatically expand the information available to public health officials, hospitals and physicians, helping save lives and allowing the healthcare system to better deal with this crisis.โ€ said Brad Pitts, Synergyโ€™s Chief Executive Officer.

Brandon Biles, Synergyโ€™s Chief Operating Officer, highlighted the speed of the new testing process. He said, โ€œWe will be able to deliver results in within one-to-two days utilizing the latest test equipment and our cutting-edge information services technology. This will help patients learn their status quickly, and allow individuals who test positive for COVID-19 to begin receiving treatment sooner.โ€

Synergy will be processing testing samples delivered to the lab from healthcare facilities and physiciansโ€™ offices only. Existing Synergy clients may order test kits through their normal online channels. Prospective customers can contact Synergy by phone at (251) 662-9760 or establish a new client relationship through Synergyโ€™s New Client link at www.synergytesting.com.

The new testing capability will utilize a ThermoFisher 7500 Fast Dx system, which is one of three systems recently given fast-track approval by the FDA under an emergency use authorization. Synergy is preparing the required test kits in its facilities in Mobile, Alabama, and will be distributing them to healthcare facilities and physicians.

About Synergy Laboratories

Synergy Laboratories is a full-service diagnostic laboratory that utilizes a wide range of innovative platforms to improve patient care. Founded in 2015, by Brad Pitts and Brandon Biles, Synergyโ€™s mission is to ethically serve the healthcare sector and give healthcare providers quality service and accurate results. In recent years, Synergy has continued to invest in the latest technology to serve their ever-growing client base.

Luminex Receives FDA Emergency Use Authorization for ARIES SARS-CoV-2 Assay to Detect Virus Responsible for COVID-19

Luminex Receives FDA Emergency Use Authorization for ARIES SARS-CoV-2 Assay to Detect Virus Responsible for COVID-19

Luminex Corporation announced that the FDA has issued an EUA for its ARIESยฎ SARS-CoV-2 Assay for rapid detection of the virus that causes COVID-19. The assay runs on the ARIESยฎ System, an FDA-cleared, sample-to-answer, automated, on-demand molecular diagnostic platform. The system is capable of running up to 144 tests per day, requiring no specialty training and minimal human interaction.

The ARIESยฎ SARS-CoV-2 Assay will allow hospital professionals to determine the appropriate course of treatment for patients suspected of having COVID-19 within approximately two hours,” said Nachum “Homi” Shamir, President and CEO of Luminex. “We are grateful to the FDA for this Emergency Use Authorization, which allows us to bring another cost-effective SARS-CoV-2 test from Luminex to labs and patients in dire need of quick, accurate results. We are scaling up production of this assay over the next three weeks to support hundreds of labs across the US and the rest of the globe. These labs are already operating the ARIESยฎ System and should be able to get up and running very quickly as we make this test broadly available.”

Luminex also launched the NxTAGยฎCoV Extended Panel last week after receiving an EUA from the US FDA and Medical Device Authorization for importation or sale for Health Canada. The panel is a high-throughput, scalable, cost-effective option for detecting SARS-CoV-2 in as many as 96 samples in approximately four hours. To provide a more complete picture of a patient’s respiratory health, the NxTAG CoV Extended Panel can also be run in parallel with the NxTAG Respiratory Pathogen Panel.

Luminex is actively supporting laboratories in the US, Asia, and Europe with their testing, and the company has expanded its manufacturing capacity to produce up to 200,000 ARIESยฎ SARS-CoV-2 tests per month, in addition to 300,000 NxTAG tests per month, with the majority of this capacity focused on SARS-CoV-2.

The NxTAG CoV Extended Panel and the ARIESยฎ SARS-CoV-2 Assay have each been funded with $642,450 of Federal funds, approximately 36% each of the expected overall cost of development, from the Department of Health and Human Services; Office of the Assistant Secretary for Preparedness and Response; Biomedical Advanced Research and Development Authority, Division of Research Innovation and Ventures under Contract Nos. 75A50120C00037 (NxTAG CoV Extended Panel) and 75A50120C00043 (ARIESยฎ SARS-CoV-2 Assay). Luminex financed the remaining $1,118,663 of each program, constituting 64% each of the total program costs.

About Luminex Corporation
At Luminex, our mission is to empower labs to obtain reliable, timely, and actionable answers, ultimately advancing health. We offer a wide range of solutions applicable in diverse markets including clinical diagnostics, pharmaceutical drug discovery, biomedical research, genomic and proteomic research, biodefense research, and food safety. We accelerate reliable answers while simplifying complexity and deliver certainty with a seamless experience.

New Tech Platform Launched by Zegami to Analyse COVID-19 X-Rays to speed up Diagnosis

Zegami, the Oxford University data visualisation spin-out, has developed a new machine learning model using x-rays of Covid-19 infected lungs, artificial intelligence techniques and data visualisation tools that could help medical professionals identify Coronavirus cases more effectively, but also potentially help provide a better idea of potential outcomes for patients, and even lead to more effective treatments.

However, to reach its full potential, Zegami needs a huge supply of Covid-19 x-rays and details on treatments used for patients and the outcomes, so it has written an open letter to The Oxford Health NHS Foundation Trust, and the NHS as a whole, asking for these images and data, and offering its services in the fight against Coronavirus.

It believes it would only take a matter of weeks to have enough images of Covid-19 x-rays for its new platform to become usable as a diagnostic tool.

Zegami says its new model could not only help identify and differentiate Covid-19 cases more easily from other lung conditions such asย  ‘bacterial pneumonia’ and ‘viral pneumonia’, it could also help predict potential outcomes for patients by comparing their Covid-19 lung x-rays with other previous patients who had similar conditions, and what eventually happened to them based on different treatment options.

In developing its new platform, Zegami has initially used images of COVID-19 x-rays from the GitHub data initiative, which was launched by Joseph Paul Cohen, a Postdoctoral Fellow from Mila, University of Montreal.ย  He is looking to develop the worldโ€™s largest collection of X-ray and CT images of Covid-19 infected lungs, to enable automated diagnosis faster and more accurately.ย 

To date, because the images used by Zegami give no details on what happened to the patients, its model can only help distinguish Covid-19 cases more easily from other lung conditions.ย ย 

Roger Noble, CEO and founder of Zegami said: โ€œCovid-19 is a huge challenge, and technology should play a key role in defeating it. We believe the model we have developed cannot only be used to help identify cases of Coronavirus more quickly, with the right visuals and information loaded on to our platform and using data visualisation and AI tools, we can help identify potential outcomes for patients by comparing their cases with former patients who had similar conditions and learning what happened to them.

โ€œHowever, to complete our project we need more data and visuals of Covid-19 x-rays and the treatments used for these case and their eventual outcomes, so we have written to the NHS asking if they would like to work with us on this project, and to see if they can provide the visuals and data we need.

โ€œThe model we develop could not only help our amazing NHS staff to make more informed decisions and potentially save lives, it could be shared around the world and play a role in helping to defeat Covid-19 on a global scale.โ€

Zegami launched out of Oxford University in 2016.ย  It is currently exploring new ideas and making new discoveries for 35 clients and counting, across an ever-growing variety of sectors.ย ย 

Bactiguard completes acquisition of Vigilenz

Bactiguard completes acquisition of Vigilenz

Bactiguard Holding AB has completed the acquisition of Vigilenz Medical Devices and Vigilenz Medical Supplies (together Vigilenz), which was announced on 4 February 2020.

All conditions precedent have been fulfilled and the first part of the total consideration, consisting of a cash payment of USD 4.5 million, has been paid. The remaining part of the consideration, 241 512 new class B-shares in Bactiguard, is subject to approval by the annual general meeting of shareholders in Bactiguard on 28 April 2020.

The cash portion has been financed through bank facilities provided by Skandinaviska Enskilda Banken (SEB), with a term of three years. At the same time, the term of Bactiguardโ€™s current bank facility with SEB has been extended by the same tenor.

The Bactiguard Board of Directors has approved the transaction and shareholders including Christian Kinch, Thomas von Koch, Jan Stรฅhlberg, The Fourth Swedish National Pension Fund (AP4) and Nordea Investment Funds, together representing approximately 66 percent of the capital and 84 percent of the votes in Bactiguard have declared that they will support the issuance of new class B-shares at the AGM.

The newly acquired companies will be consolidated in Bactiguard’s financial accounts from March 2020. At the same time, the integration of the companies has been initiated, which means, among other things, that the product portfolios will be sold through both companies’ distribution networks.

In the fight against the Corona virus, Bactiguard donates infection prevention to China

In the fight against the Corona virus, Bactiguard donates infection prevention to China

In the fight against the Corona virus, Bactiguard donates products for infection prevention to Chinese hospitals, at a market value of over 2 million SEK.

โ€œTo help fight the new corona virus (covid-19) and protect the most severely ill patients, we will donate products from Bactiguardโ€™s and Vigilenz’s combined product portfolios to Chinaโ€, says Stefan Grass, Chief Medical Officer and Deputy CEO. ย 

โ€œHydrocyn aqua is a water-based product that kills bacteria, fungi and virus within seconds without damaging or irritating the body. In the past, it has proven to have a powerful effect on earlier versions of the Corona virus and can thus be very useful for prevention of both the general public and healthcare professionals. Further, our catheters for infection prevention protect patients against the bacterial infections that often come as a complication of viral infections,โ€ continues Stefan Grass.

HYDROCYN aquaยฎ is a pH-neutral and water-based product that, unlike alcohol and chlorhexidine, isnโ€™t toxic or harmful to the body. The active substance is hypochlorous acid (HOCl) which kills bacteria, fungi and virus within seconds. HYDROCYN aquaยฎ is included in Bactiguardโ€™s portfolio of products following the acquisition of Vigilenz and it is documented that the product kills 99.9% of previous variants of Coronavirus within 15-30 seconds.

HYDROCYN aquaยฎ is CE marked (EU approved) and FDA approved in the US.

Bactiguard develops and provides infection prevention solutions which reduce the risk of healthcare associated infections. In viral infections, the body’s immune system is under stress, which increases the risk of secondary bacterial infections. Bactiguard’s unique coating prevents bacteria and other microbes from adhering to the surface of, for example, catheters, which reduces the risk of biofilm formation that lead to infections.

Recently, Bactiguard completed the acquisition of Malaysian Vigilenz, a manufacturer and supplier of medical devices and consumables, primarily within wound care and infection prevention, where HYDROCYN aquaยฎ is an important part of the product portfolio.

World Health Organization and Tencent Deepened Collaboration to Fight Against COVID-19

World Health Organization and Tencent Deepened Collaboration to Fight Against COVID-19

Tencent Holdings Limited , announced to deepen collaboration with the World Health Organization (WHO) via a US$10 million donation to WHO’s COVID-19 Solidarity Response Fund, and an agreement to open source our digital health solutions to assist the global fight against the pandemic.

WHO Director-General Dr. Tedros Adhanom Ghebreyesus, and Tencent President Martin Lau made the announcement via video conference.

“I warmly thank Tencent for its generous contribution to the COVID-19 Solidarity Response Fund. I look forward to the collaboration with Tencent on promoting the use of digital health tools in the fight against COVID-19 and for a healthier, safer, fairer world,” said Dr. Tedros.

“The world is facing unprecedented challenges and needs to come together with great solidarity. WHO is leading and coordinating the global efforts, supporting countries to combat the pandemic. Tencent believes that global solidarity will help all of us fight the spread of COVID-19, and we will open source our digital health solutions in addition to making a donation to achieve this shared mission,” said Martin Lau, President of Tencent.

Announced last month by WHO, the COVID-19 Solidarity Response Fund will help all countries, particularly those most vulnerable, at-risk, and with the weakest health systems, to prepare for and respond to the COVID-19 crisis by rapidly detecting cases, stopping transmission of the virus, and caring for those affected.

The US$10 million contribution from Tencent is part of its US$100 million Global Anti-Pandemic Fund, which was established in March to support international efforts to combat COVID-19. It has already helped supply urgent medical gear, such as masks, personal protective equipment, and ventilators, to hospitals and front-line healthcare workers around the world.

In addition to the donation, Tencent will also provide technology support to combat the pandemic. Tencent Health is open sourcing the international module in its COVID 19 WeChat Mini Program, making critical information on the pandemic freely available worldwide. The COVID-19 Symptoms Self-Triage Assistant, a self-evaluation tool backed by AI technology, is also now available to people around the world.

About Tencent

Tencent uses technology to enrich the lives of Internet users. Our communication and social platforms, Weixin and QQ, connect users with each other and with digital content and services, both online and offline, making their lives more convenient. Our targeted advertising platform helps advertisers reach out to hundreds of millions of consumers in China. Our FinTech and business services support our partners’ business growth and assist their digital upgrade.

Tencent invests heavily in talent and technological innovation, actively promoting the development of the Internet industry. Tencent was founded in Shenzhen, China, in 1998. Shares of Tencent (00700.HK) are listed on the Main Board of the Stock Exchange of Hong Kong.

BioIVT Opens New Blood Donor Center to Support Boston-area Research into COVID-19 Therapies, Vaccines and Diagnostics

BioIVT Opens New Blood Donor Center to Support Boston-area Research into COVID-19 Therapies, Vaccines and Diagnostics

BioIVT, a leading provider of research models and services for drug and diagnostic development, announced the opening of its new blood donor center on the Tufts University campus in Medford, MA to support academic and pharmaceutical researchers involved in COVID-19, cell and gene therapy research.

โ€œBioIVT wants to play a leading role in supporting COVID-19 research efforts and blood donations are a vital resource for the research and development of new therapies, vaccines, and diagnostics. We have many yearsโ€™ experience developing blood products, including blood-derived immune cells for cell and gene therapy research, and we want to make that expertise count,โ€ said BioIVT CEO Jeff Gatz. โ€œResearchers recognize and appreciate BioIVTโ€™s rapid response and commitment to high quality, fresh blood products and this new donor center will allow us to offer those attributes and services to additional US clients.โ€

BioIVTโ€™s new Boston blood donor center is its seventh. The company has similar facilities located in California, Tennessee and Pennsylvania to serve US clients and in London, UK for EU-based clients.

โ€œWhile the initial focus at our Boston donor center will be on delivering fresh blood, leukopaks and buffy coats within hours of collection, we plan to add more capabilities and donors over time,โ€ said Jeff Widdoss, Vice President of Donor Center Operations at BioIVT.

Leukopaks, which contain concentrated white blood cells, are used to help identify promising new drug candidates, assess toxicity levels, and conduct stem cell and gene therapy research. They are particularly useful for researchers who need to obtain large numbers of leukocytes from a single donor.

BioIVT blood products can be supplied with specific clinical data, such as the donor age, ethnicity, gender, BMI and smoking status. Its leukopaks are also human leukocyte antigen (HLA), FC receptor and cytomegalovirus typed. HLA typing is used to match patients and donors for bone marrow or cord blood transplants. FC receptors play an important role in antibody-dependent immune responses.

 

About BioIVT

BioIVT, formerly BioreclamationIVT, is a leading global provider of research models and value-added research services for drug discovery and development. We specialize in control and disease-state biospecimens including human and animal tissues, cell products, blood, and other biofluids. Our unmatched portfolio of clinical specimens directly supports precision medicine research and the effort to improve patient outcomes by coupling comprehensive clinical data with donor samples. Our PHASEZEROยฎ Research Services team works collaboratively with clients to provide target and biomarker validation, phenotypic assays to characterize novel therapeutics, clinical assay development and in vitro hepatic modeling solutions. And as the premier supplier of ADME-toxicology model systems, including hepatocytes and subcellular fractions, BioIVT enables scientists to better understand the pharmacokinetics and drug metabolism of newly-discovered compounds and their effects on disease processes. By combining our technical expertise, exceptional customer service, and unparalleled access to biological specimens, BioIVT serves the research community as a trusted partner in elevating science.

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