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.
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.
Triomics combines the most advanced clinical trial tracking software with a global network of supersites and partners to deliver rapid, cost-effective, high quality clinical trials that pass even the most rigorous regulatory scrutiny.
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.
Stop the Drop ‒ Reducing patient drop-out rates
5thPort is a Cloud-based digital Patient Engagement and e-Consent solution built to help Contract Research Organizations (CROs) and Research Sites address four primary challenges in Clinical Trials including Decentralized Clinical Trials (DCTs).
5thPort is a better way to engage patients, explain your expectations, manage their consents and solidify your Clinical Trial Compliance.
Aspen Insights, a next generation technology provider, defines the state-of-the-art in applied data science, artificial intelligence, and machine learning for health and human performance.
Clinical.ly is a technology company with the mission to provide clinical trials software that puts you in control. Our goal is to work closely with the research community and incorporate customer feedback into everything Clinical.ly does. We aim to bring the latest advancements in intuitive, web-based technology to clinical research organization enabling them to better serve patients and sponsors.
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.
Helios Clinical Research has gathered a world-class clinical development team that engages patients and physicians to simplify their research journey to deliver.
We work with each sponsor independently to develop a customized recruitment plan to meet the specific needs of their protocol so that we can deliver the data they require
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.
VigiLanz is an award-wining safety, quality, and risk platform that enables healthcare providers to quickly capture, monitor, and act on information that enhances patient safety and reduces organizational risk.
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.
Encore Research Group
Interspond, LLC is a Trial Management Organization (TMO) established in 2003 that works with a hybrid network of exclusive and affiliated multi-therapeutic sites across the country. As such, we seek to identify study opportunities for the sites with which we work. Once identified, we query the sites, submit them for consideration for participation, facilitate the study start-up process and negotiate the contract and budget.
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.
Since 1994, CenterWatch has been the recognized global leader in providing clinical trials information to professionals working at sponsors, CROs, research sites and niche service providers.
Today, CenterWatch delivers critical industry insights to 150,000 life science executives every week through its newsletters, conferences, webinars, books, in-depth market surveys, industry profiles and clinical databases. And millions of patients and caregivers start their search for clinical trials with CenterWatch, with one of the largest clinical trial databases on the internet, CenterWatch iConnect.
To learn about the products CenterWatch offers click here.