Do you want to spread the word about your organization’s solutions and services to those in attendance at the 11th Annual Clinical Trial Billing & Research Compliance Conference? 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 our needs.
To learn more about these opportunities, please contact Andrew Sinetar, Managing Director of Strategic Business Development, at firstname.lastname@example.org or 212-400-6237.
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.
CITI Program at the University of Miami
The Collaborative Institutional Training Initiative (CITI Program) provides web-based research ethics and compliance education. Our materials cover a number of key regulatory and ethical areas including:
- Animal Care and Use
- Biosafety and Biosecurity
- Clinical Research Coordinator
- Clinical Trial Billing Compliance
- Conflicts of Interest
- Disaster Planning for the Research Enterprise
- Export Compliance
- Good Clinical Practice
- Good Laboratory Practice
- Human Subjects Research
- Information Privacy and Security
- Responsible Conduct of Research
For subscription information, please contact email@example.com or visit www.citiprogram.org.
Clinical Conductor is the industry’s first collaborative and configurable CTMS for organizations managing or executing clinical trials built to have the most in-depth billing and research compliance functionality available. Clinical Conductor also provides users with the specific features and the functionality they need to effectively collaborate with or among sites and other partners, generate in-depth and valuable trial data and reports, and maximize profitability. Used by more than 1,800 organizations around the world, Clinical Conductor provides organizations with the tools they need to continue to raise the bar in clinical research.
Complion is a document management and workflow platform for clinical research sites. Built by clinical researchers for clinical researchers, it transforms the way clinical trial documentation is maintained. Leading physicians, hospitals, academic medical centers, health systems and cancer centers around the country leverage Complion to reduce regulatory burden, improve compliance and streamline operations.
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.
Working with hospitals, health systems and academic medical centers, GuideStar optimizes clinical research through expert guidance and support. From trial start-up services resulting in quicker trial initiation to comprehensive site evaluations that ensure the most efficient structure is in place, GuideStar is your resource to improve research operations, compliance and finances.
IntegReview IRB provides biomedical and social-behavioral ethical review for hospitals, institutions and pharma/device companies in the U.S., Latin America, Japan and Canada for everything from industry-sponsored, federally funded or investigator-initiated projects to daily meetings. We offer customer support 24/7 with 24-48 hour document turnaround. Our online real-time document management system is fully transparent, so your team can access all your projects. We are quality-driven, responsive, experienced and flexible while maintaining ethical integrity. Fully accredited AAHRPP. Woman-owned independent IRB since 1999.
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.
Qcare, a site services provider backed by QuintilesIMS, a pioneer of clinical research services, has the deep expertise and experience to solve site administrative challenges and ensure that sites can maintain their focus on patient care while accessing the largest portfolio of clinical trials in the industry.