RealTime provides investigative sites the tools they need to manage all aspects of their clinical trials with web-based software. All phases of study execution are easily managed with RealTime-CTMS, the ultimate clinical trial management system. Features include study feasibility and business development tracking, digital marketing and recruitment modules, scheduling and integrated TEXT messaging, financial accounting for billing, plus collections and payables to include RealTime-PAY, a reloadable patient stipend card system. Our latest feature, RealTime-eDOCS, allows investigative sites to go paperless with the first-ever CTMS-Integrated eRegulatory system.
WCG is the world’s leading provider of services that measurably improve the quality and efficiency of clinical research. As the industry’s first clinical services organization (CSO), WCG enables sites, biopharmaceutical companies, and CROs to accelerate the delivery of new treatments and therapies to patients, while maintaining the highest standards of human subject protection. For more information, please visit www.wcgclinical.com or follow us on Twitter or LinkedIn at @WCGClinical.
Inteliquet™, an IQVIA business, enables cancer research providers with the technology and support services to accelerate trial feasibility and patient matching. The OncWeb™ platform harnesses various sources of clinical data and reduces the burden of manual feasibility, matching patients to complex cancer trials with great speed and precision.
Aspen Insights is a data science and machine learning technology firm principally engaged in the research, design, development, and integration of advanced healthcare analytics systems, products, and services. Aspen brings innovation to the clinical research space through their EMR-agnostic, scale-wide semantic search platform, Aspen Forge.
Aspen Forge:
- provides a means to quickly identify optimal trial candidates in a fraction of the time compared to traditional methods.
- makes structured & unstructured data searchable for thorough clinical analysis of patient records.
- enriches clinical text to enable abstract concept search, for example: “exclude all patients currently on an antidepressant”.
- enables accurate feasibility analysis through simulation-based and risk-adjusted enrollment projection.
- fuses data from multiple EMRs and therapeutic areas to support centralized recruitment
- requires no customization for various therapeutic areas.
- includes patient outreach tracking and native CTMS integration.
Clinical.ly. Now there’s an easier way to address regulatory obligations and compliance challenges. As regulations become more burdensome and labor costs rise, Clinical.ly solutions can help you stay ahead.
Clinical Research IO. Powerful, all-in-one "e-source" and site operation software built specifically for clinical research sites.
Complion's mission is to transform the way clinical trial regulatory documentation is created and maintained, thus fostering greater regulatory compliance, better protection of human subjects, and easier cross- and intra-institutional collaboration. We seek to unleash medical innovators to better focus on improving patient outcomes.
Curebase is a full-service CRO and eClinical Platform for running distributed clinical trials using technology to enroll and manage patients wherever they live. Our software platform is built for remote research with online consent, remote monitoring, and at-home data capture. We have experience executing clinical trials for med-devices, diagnostics, and SaMD.
Whether you are brand new or managing hundreds of clinical research trials, choosing the right software is crucial to running successful clinical research sites. Most sites use a CTMS (Clinical Trial Management System) to track patients, schedules, financial budgets, and recruitment efforts. A CTMS should enable your staff to work faster, help you maintain compliance ClinasystNG is the most user-friendly web-based CTMS on the market. It is designed by research sites for research sites to navigate clinical trials successfully. Not only does ClinasystNG include all the essentials for running clinical trials, but it also excels as the most user-friendly, intuitive, and budget-conscious system allowing your organization to flourish with ClinaystNG features in Patient Management, Financial Administration, Scheduling Simplicity, Research Ready Recruitment, Team Collaboration, Secure Document Storage, and Training. Please stop by our booth to learn how you can save 10% off your first year!
Factor, formerly Axiom Managed Solutions, is the leader in solutions for complex legal work at scale. Factor combines expert legal resourcing and market know-how with the process efficiency, smart legal technology, and data-driven project management of New Law to bridge a huge gap in the market. The company is comprised of more than 500 professionals.
Florence helps over 7,200 research sites, sponsors and CROs across 27 countries advance research through purpose-built technology. Florence transforms clinical trials with the #1 platform for electronic document workflows and remote site access.
Veeva SiteVault is the only unified solution connecting sites with sponsors and patients to run digital trials. Improve your research operations and connect to 400+ sponsors that use Veeva Clinical applications.
CITI Program offers an easy-to-manage turnkey solution that organizations can use to train entire groups of researchers, personnel and students affordably. Individuals can also purchase courses to advance their knowledge and for professional development.
Deep 6 AI uses artificial intelligence and natural language processing on medical records so you can find and validate the patients you need to run a successful trial—in a matter of minutes. Designed to put recruitment power into the hands of researchers, Deep 6 transforms trial criteria into an AI-powered search query. The tool then lets research staff search both structured and unstructured medical data—like physician’s notes and pathology reports—so they can find and screen more, better-matching patients for their most complex trials more quickly. The Deep 6 AI platform is EMR-agnostic and allows users to identify, screen, and recruit patients in a HIPAA and IRB-compliant manner.
ImageBloom, Inc. is a full-service marketing and patient recruitment agency specializing in digital advertising. Our global client base includes healthcare practices, clinical research sites, and CROs/sponsors. We understand what it takes to drive enrollment and are committed to providing unique, creative solutions using the most cutting-edge platforms.
NeuroCatch inc. is a neurotechnology company that develops deployable, cost-effective and non-invasive tools to objectively evaluate and optimize treatment for brain health. The company’s flagship technology is the NeuroCatch® Platform. The NeuroCatch® Platform allows cognitive evaluation in research settings as well professional healthcare facilities including clinics and remote deployments.
PRIM&R advances high ethical standards in research, providing education to biomedical, behavioral, and social science research professionals.
Sullivan Insurance Group is a leading nationwide insurance and risk management provider for companies involved in the clinical trial service industry, with over 20 years of experience. We provide global comprehensive solutions to over 400 sponsors, contract research organizations, site management organizations, academic medical centers, IRBs, e-clinical organizations, and research sites.
The Patient Recruiting Agency™ is a full-service global patient recruiting and retention company supporting Investigators, CROs, and Sponsors. Over the past 20 Years, TPRA has recruited over 10,000 patients of all genders, ages, and races for over 150 therapeutic indications and campaigns in multiple languages.
BEKHealth empowers healthcare organizations of all sizes to quickly enter or expand clinical research. The BEKHealth solution is the most advanced system for ingesting EMR data, conducting trial feasibility, and identifying protocol-eligible patients for clinical trials. Our solution covers more than 95% of the trial protocol which leads to unprecedented accuracy and operational improvement. By taking out manual tasks, researchers can allocate more time to enroll and see patients.
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