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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.
Complion’s mission is to reinvent site regulatory and document management by eliminating human error and redundant work to achieve maximum efficiency and compliance. We are the first and are the largest eRegulatory platform built for sites, health systems, academic medical centers, and cancer centers.
Forte – Now an Advarra Company
Forte provides software and services in the critical areas of clinical trial management, clinical data management and research administration for cancer centers, academic medical centers and health systems.
With a strong belief in community, collaboration and standards-based development, Forte also facilitates the Onsemble Community, a customer-exclusive group for peer networking, best practices and support. Twice a year at the Onsemble Conference, clinical research professionals meet in person and discuss the latest challenges and solutions in clinical research.
Forte provides all research professionals complimentary blog articles, eBooks, webinars and more to support continuous learning on industry topics.
Forte was recently acquired by Advarra, the premier provider of institutional review board (IRB), institutional biosafety committee (IBC), and global research compliance consulting services. The combined organization leverages mutual strengths in supporting the research community with client service, regulatory expertise, and technology-enabled efficiencies to accelerate innovation, streamline research operations, support faster study start-up, and help make research altogether better.
GuideStar Research works with hospitals, health systems, and academic medical centers around the country to build and support clinical research programs. From helping organizations develop or refine a clinical trial strategy to providing support for coverage analysis, regulatory start-up, contracts, budgets, and more, our experienced team helps to ensure optimal results for research programs.
Huron is a global consultancy that helps our clients drive growth, enhance performance and sustain leadership in the markets they serve. We partner with them to develop strategies and implement solutions that enable the transformative change our clients need to own their future.
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.
WCG PFS Clinical is dedicated to helping research institutions improve the management of clinical trials from start-up to final payment. We provide on-demand contract, budget, coverage analysis, and financial management services as well as consulting/training. By partnering with WCG PFS Clinical, you get experts that support your research program without the cost of hiring, training, or retaining, and a “right-sized” team that can ebb and flow with your workload.