ClinEdge and BTC Network provide a full range of clinical and outsourced business services to clinical research sites, pharmaceutical companies and CROs. Together, ClinEdge & BTC Network are comprised of : two global networks of research clinics with over 1,000 physician investigators, a division of site financial services, and a division of patient recruitment/ retention services which include online engagement and advertising, a national patient database, patient travel concierge, national and local support and advocacy communication, and in-house call center, among other services. With experience across over 300 indications across all divisions, our teams are prepared to assist you in all aspects of the clinical trial industry.
Clinical.ly provides differentiated technological solutions to the clinical research industry, helping research facilities focus on conducting studies as efficiently as possible. We’re working hard to provide modern, intuitive software that frees up resources and reduces headaches. As trials keep evolving in complexity, it is becoming more apparent that the same old procedures aren’t keeping up. Inspection findings are much more costly than adopting the right technology, procedures and best practices.
The clinical trials industry is ready for better tools to help stay ahead of the evolving demands of sponsors and regulators.
We work closely with clinical trials facilities to understand their SOPs and provide solutions to help address their nuanced needs. By integrating your proprietary workflows, we help remove barriers to adoption and help you focus on your primary responsibilities. Free your medical staff to focus on the jobs you hired them to do.
eRegBinder by Clinical.ly is a purpose-built solution designed to help organizations meet regulatory compliance requirements in clinical trials. The system reduces mistakes by tracking required documents, signatures, and timelines, as well as offering automatic alerts on missing data. With electronic delegation and training logs, and remote monitoring access your time spent on regulatory compliance is minimized, helping you avoid spending employee time on fixing mistakes, omissions or missing information.
An SCRS Global Impact Partner™
With more than 1,500,000 registered healthcare professionals worldwide, growing at an average of 15,000 – 22,500 new registrants per month, BlueCloud® has the fastest growing networks in healthcare and clinical research. A global networking technology that enables industry stakeholders to create new and efficient business models that improve patient care by implementing standards and eliminating waste and fraud. This ecosystem allows the exchange of “real-time” information required by regulatory agencies. BlueCloud acts as the catalyst for standardizing global programs like the NIH Stroke Scale (NIHSS), Modified Rankin mRS, Barthel Index (BI), Suicidality Scale (C-SSRS) and other diagnostic neuroscience programs. Let’s save lives, together!”.
For more information visit www.healthcarepoint.com
When you need to find qualified patients for clinical trials, it’s easy to get lost in the process. Mapping out a direction and taking the right path is critical. That’s why The Patient Recruiting Agency™ (TPRA) is here. We are metrics driven and our focus is on the development and deployment of targeted recruiting and retention strategies and tactics on a global level. We specialize in the production and placement of customized, direct-to-patient outreach and technological solutions to support Sponsors, CROs, SMOs and Investigators. Since 1999, we’ve completed over 2,500 recruiting campaigns for more than 150 different indications in multiple languages and countries.
Think of TPRA like your very own patient recruiting and retention GPS. We’ll navigate you through the bumpy and windy roads toward successful patient recruiting and retention. We will manage the entire journey IN-HOUSE, which provides you with a single point of accountability, greater cost efficiencies, greater control of services and timelines, increased flexibility and shortened reaction time. Our solutions generate a greater response from a higher percentage of qualified patients at a lower cost per patient randomized on time and within budget. Our experience coupled with our accountability to metrics and our approach of having all major tactics performed IN-HOUSE are the reasons we are The Leader in Successful PATIENT RECRUITING & RETENTION.
Save time and simplify your regulatory tasks with Complion, the industry’s leading eRegulatory solution designed to make your life easier.
• Eliminate paper binders
• Collect eSignatures
• Track expirations and outstanding tasks
• Ensure 21 CFR Part 11 Compliance
• Standardize filing and naming conventions
• Simplify remote monitoring
Experience the Complion Difference
• Trusted by 80+ sites to manage over 4,000 studies.
• Accessed by 1400+ monitors from 170+ sponsors and CROs!
• The only system designed to automate repetative tasks
• Best practices and industry standards
• Template policies and SOPs to ensure your long-term success
• Maximize sponsor acceptance and reimbursement
• Largest and most experienced team on the market
Sign up for a free demonstration today!
The Leader of Global Clinical Trial Management Sytems
RealTime Software Solution is a global leader in SAAS-based Clinical Trials Management Systems for Sites, Sponsors, and CROs. RealTime is also the only CTMS vendor that can offer a complete suite of solutions into a seamless platform, SOMS (Site Operations Management System).
SOMS includes the industry-leading CTMS, SitePAY, TEXT, eDOCS, and eSOURCE which is accessible through an easy-to-use MobileAPP. RealTime also has the most advanced multi-site and site network enterprise systems available anywhere.
With an international customer base, multiple integrations with other vendors, advanced recruitment systems, intuitive monitoring portals, Outlook integration, a powerful MobileAPP and more; the team at RealTime has made a significant impact on the efficiency of the clinical research process from start to finish.
Our History
RealTime-CTMS was initially developed in 2005 by experienced clinical research professionals. Today, the leadership and stakeholders of RealTime Software Solutions are some of the most prominent knowledge and opinion leaders in our industry. RealTime will continue to expand its service offerings and the delivery of disruptive new technologies that will shape the future of clinical research.
