Do you want to spread the word about your organization’s solutions and services to potential clients who will be attending this event? Take advantage of the opportunity to exhibit, underwrite an educational session, host a networking event or distribute promotional items to attendees. ExL Events will work closely with you to customize a package that will suit all of your needs. To learn more about these opportunities, please contact Andrew Sinetar, Managing Director, Business Development, at 212-400-6237 or firstname.lastname@example.org.
At Bad Rabbit, we use our tall ears to listen closely for how we can help your institution meet strategic goals, with a focus on long-term usability and ease of use. Our team, made up of only senior-level experts, works exclusively with academic and medical research institutions, so we’re uniquely positioned to help you to get the most out of your IRB, Grants, IACUC, IBC, COI and other research compliance sites, whether that means implementation, custom development, integration with other platforms, or even the ongoing day-to-day management of your sites.
Barrington James are a Global specialist recruitment consultancy with offices in Europe, the USA, and Asia-Pacific that work across the Healthcare sector. Our structure, with separate divisions and dedicated consultants for the markets we serve, ensures a thorough, professional and intelligent approach to both permanent and interim solutions. Our tailored methodologies include Contingency database search and executive search.
Clinical Conductor CTMS, offered by Bio-Optronics, is the premier family of clinical trial management systems for clinical research professionals. Solving today’s most challenging problems, Clinical Conductor CTMS is the proven research project management tool used by over 1,600 research organizations around the world.
Research sites benefit from Clinical Conductor Site CTMS and its versatile tools designed specifically for the needs of sites. Clinical Conductor Enterprise CTMS provides AMCs, SMOs, CROs and healthcare networks the tools and communication that is needed for trial success. With a heavy focus placed on billing compliance functionality, Clinical Conductor CTMS is the necessary tool for any research organization.
Additionally, Clinical Conductor CTMS ensures regulatory compliance, improves study execution speed, collects more accurate data and increases your profitability, all from the very first day. Our compassionate and expert team of service specialists and engineers are there to support you and continually deliver enhancements, customizations and integrations to meet your specific needs.
Bio-Optronics, Inc. is a software and services provider specialized in solutions to help healthcare and life science professionals manage and optimize workflow, thus enhancing quality, productivity and patient and staff satisfaction. Since 1985, Bio-Optronics has demonstrated leadership in innovation, expertise in workflow and integration and a focus on unparalleled customer service.
For more information about how Clinical Conductor CTMS can help you, please visit our website:
The process of conducting a comprehensive Medicare Coverage Analysis is an essential part of developing a clinical trial budget for research sites. BRANY’s experts provide end-to-end analysis, budgeting and sponsor contract negotiations for clinical trials. We work with investigators and research offices to develop specific and detailed processes to ensure compliance.
Cerner’s health information technologies connect people, information, and systems at more than 25,000 provider facilities worldwide. Recognized for innovation, Cerner solutions assist clinicians in making care decisions and enable organizations to manage the health of populations. The company also offers an integrated clinical and financial system to help healthcare organizations manage revenue, as well as a wide range of services to support clients’ clinical, financial and operational needs. Cerner’s mission is to contribute to the systemic improvement of health care delivery and the health of communities.
CITI Program, a division of BRANY, is a leading provider of research ethics and compliance education. Our web-based training materials serve millions of learners at academic institutions, government agencies, and commercial organizations in the U.S. and around the world. Learn more about our content offerings at www.citiprogram.org.
Complion is a flexible, enterprise platform used by research sites to optimize the management of regulatory documents. Built by clinical researchers, Complion removes walls between physicians, administrators and staff by intelligently providing secure access to the right document when they need it. Leading sites, hospitals, health systems, academic medical centers, and cancer centers use Complion to streamline operations and improve compliance.
Forte Research Systems
Forte Research Systems has been developing software for clinical research organizations since 2000. Forte’s OnCore Enterprise Research® system supports efficient research, compliance, data management and budgetary processes at academic medical centers, cancer centers, and healthcare systems across the U.S. The billing compliance module in the OnCore system helps centralize and communicate information across teams, supporting accuracy and consistency in processes. Forte also recently unveiled the Forte Research Ecosystem, a living, interconnected network linked through people, process, and technology. The Ecosystem was developed through collaboration with Forte customers and the clinical research community to accelerate life-saving preventions and therapies with standards-based technology.
GuideStar works with hospitals, health systems and physician practices around the country to build and support clinical research programs. From helping organizations incorporate a clinical trial strategy to providing management guidance and support, our service delivery is based on operational and financial best practices to ensure optimal results for research programs.
Kelly Willenberg & Associates
Kelly Willenberg & Associates is a full service research compliance organization serving clients on improving operations. She employs technologies to improve operational aspects of compliance based on client needs. She assists in implementation of billing compliance programs, offers training seminars, builds coverage analysis and helps with process improvement. She can also assist with process improvement, quality assurance and assessing vulnerabilities in all aspects of research compliance.
PFS Clinical provides administrative solutions that focus on the unique and complex challenges inherent to clinical research. Partnering with PFS Clinical will decrease study start-up times, overhead costs, and internal training, while truly allowing personnel to refocus their attention to quality patient care. Our unique knowledge and expertise differentiate our business practices and provide unparalleled solutions for academic medical centers, community hospitals, and dedicated research facilities.