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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.
Bio-Optronics is the creator of Clinical Conductor, the leading CTMS for collaboratively managing multiple clinical trials and sites. Used by more research sites around the world than any other CTMS, Clinical Conductor is managing over 40,000 studies. Clinical Conductor is part of the CCTrialSuite, a comprehensive set of integrated, patient-centric clinical research management and eClinical products available from a single supplier that streamline research operations, ensure compliance and enhance research business growth. Adding to the power of Clinical Conductor in the suite are a growing set of new solutions, including Part 11 compliant CCeReg document management, CCeSource real-time data capture, mobile friendly CCeConsent, instant payment CCPay and 2-way texting CCText solutions that will have the most seamless CTMS integration in the industry.
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.
Florence advances clinical trials through software for managing document and data flow between research sites and sponsors. Florence eBinders is trusted by 5,000+ Investigators to manage eRegulatory/eSource for over 1,200 studies, Florence eTMF is the most flexible eTMF on the market with a wide range of innovative features, and Florence eHub is revolutionizing site-sponsor connectivity in a virtual site workspace for site oversight, monitoring, startup, and document exchange.
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.