Healthcare
PRODUCTS
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Build batches that scale easily scale your batches up or down according to size, complexity, or customization.
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Unexpected downtime can drastically impact your organization’s ability to service customers and hinder innovation. With Waters FlexCHOICE: mySystem Coverage*, you can safeguard against lost productivity and unexpected downtime and spend more time on what matters most – your customers and your research.
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FectoVIR®-LV
Lentiviral vectors are recognized to be the carrier of choice for allogenic or autologous cell therapies (such as CAR-T) because of its capacity to permanently integrate viral genome into host cell DNA. To produce those vectors, cell therapy producers generally use a transient transfection system that is scaled-up during process development phases. FectoVIR®-LV is the next generation of transfection reagent, free of animal component, designed to improve LV productivity in HEK-293 cell systems. FectoVIR-LV is made for large scale manufacturing with reduction of the complexation volume and increased complex stability. The benefits that FectoVIR-LV bring allow to increase number of doses produced per batch to treat more patient, while decreasing manufacturing costs.
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THUNDER Imager Live Cell & 3D Assay
Decode 3D biology in real time*
With THUNDER Imagers you begin every experiment with confidence. They are your solution for advanced 3D cell culture assays, whether you want to study stem cells, spheroids, or organoids.
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Why Implement an FDA 21 CFR Part 11 Pharmaceutical Software System?
Learn from industry practitioners and experts why implementing an FDA 21 CFR Part 11 Software System is so essential. Within a year of 21 CFR Part 11 first going into effect MasterControl introduced the industry's first document management software solution specifically designed to help life sciences organizations comply with FDA regulations, the regulations delineated in 21 CFR Part 11 in particular. MasterControl's solutions streamline and automate GxP processes and facilitate effective management of document control, change control, training control, audits, corrective/preventative action (CAPA), customer complaints, and other quality and business processes, all under a single Web-based platform.
WHITE PAPERS AND CASE STUDIES
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Control Your Data Flow, Control Your Trial
The surge of healthcare data threatens to cripple healthcare organizations. But an effective data flow environment can get it under control.
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Beyond Integration: Flexible Orchestration Of IRT And eCOA Solutions
Consider how integrated response technologies and electronic clinical outcomes assessments can improve configurability, study start-up, and flexible mid-study changes.
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8 Best Practices For Compliant And Quick Software Validation In The Cloud
Learn how to significantly lighten the software validation load for your cloud environment system with these eight key practices.
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Water Utility Enhances Reliability With Integrated Technology Upgrades
For public utilities that provide water while maintaining the physical infrastructure, it is critical to ensure reliable uninterrupted service and data integrity. This includes water metering/billing, compliance reporting, IT network cybersecurity, physical security of local and remote sites, and data collection for rate cases.
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Regulatory Guidance On GMP Software
Explore the regulatory requirements for software in a biopharmaceutical GxP environment and why software is invaluable for creating an audit trail, reporting, and automating regulatory-related tasks.
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Life-Saving Treatments Reach Patients Faster
Follow LivaNova's journey as they search for a solution to simplify and streamline trial initiation and management processes to expedite the delivery of life-saving devices.
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How Sponsors And CROs Can Fully Benefit From The Permanent Shift To Decentralized Home-Visit Clinical Trials
To aid sponsors and CROs in fully realizing the benefits of decentralized clinical trial methods moving forward, this whitepaper extracts the lessons learned from the pandemic and their implications for clinical trials now and in the future.
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eSource: The Evolution Of Clinical Trial Data Capture, Monitoring, And Management
Learn about the rapid rise of eSource and how it is quickly displacing traditional paper-based data sources.
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How Effective Training Management Can Help You Prevent Quality Issues
Training defines the quality of the single most important asset of your organization: your employees. A good training management process serves as a preventative measure against poor quality.
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DC Water's Digital Twin Solution
Explore how operational and financial resilience can be improved by implementing a water infrastructure digital twin.
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Logistics, Transport Challenges Require Complex Solutions
The pandemic created additional obstacles for the clinical supply chain. Ensuring continued clinical trial operation requires an optimal management solution for clinical material supply.
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How Service Providers Can Create Momentum In An Established Brand
To promote brand growth, companies must identify which brand components are succeeding and which may be falling short, as well as understand how these dynamics manifest in the larger organization’s successes and failures.
NEWS
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Adaptive Announces Launch Of Epic Integration For clonoSEQ®9/13/2023
Adaptive Biotechnologies Corporation (Nasdaq: ADPT), a commercial stage biotechnology company that aims to translate the genetics of the adaptive immune system into clinical products to diagnose and treat disease, today announced that clonoSEQ® is now available to health care providers as a fully integrated test in Aura, Epic’s specialty diagnostics suite.
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CEA-Leti Papers At Photonics West Report Progress Towards MicroLED Bandwidth And Efficiency Improvement1/24/2024
CEA-Leti will present two papers on its microLED technology advances at Photonics West 2024 about making matrices of LEDs with increased data-rate density, and strategies to reduce their efficiency loss at small sizes.
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QHSLab, Inc. Announces Representation Agreement With Healthcare Information Technology Specialists Of Florida2/16/2023
QHSLab, Inc. (the “Company”) (OTCQB: USAQ), a company focused on providing clinicians with tools to leverage proactive, value-based healthcare solutions through emerging digital health and point-of-care technologies, announces entry into a representation agreement with Florida based, Healthcare Information Technology Specialists, LLC.
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Andes Technology Collaborates With LDRA To Deliver Integrated Tool Suite For Safety-Critical Software On Andes RISC-V CPU Solutions1/19/2023
Andes Technology (TWSE: 6533; SIN: US03420C2089; ISIN: US03420C1099), a leading supplier of high efficiency, low-power 32/64-bit RISC-V processor cores and founding premier member of RISC-V International, today announced the integration of AndeSight™ IDE with LDRA tool suite. The integration with LDRA’s comprehensive set of software standards compliance, testing, and verification tools helps developers to develop and manage applications in increasingly complex and safety-critical industries such as aerospace, automotive, railway, industrial, and medical on Andes RISC-V CPU solutions.
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CareCloud Launches Redesigned And Enhanced Comprehensive Solution For Rehabilitation And Therapy Practices12/11/2023
CareCloud, Inc. (Nasdaq: CCLD, CCLDP, CCLDO), a leader in healthcare technology solutions for medical practices and health systems nationwide, today announced the launch of its redesigned and enhanced Therapy Solution Suite, a cutting-edge, all-in-one web-based solution poised to transform therapy and rehabilitation practice management by offering an unparalleled combination of financial, operational, and clinical efficiency.