July 14, 2015 – ROCHESTER, NY – The latest iteration of Clinical Conductor CTMS continues the proven strategy of providing research organizations with the most in-depth features and functionality available, further distancing the application from others in the industry, which fail to provide the tools necessary for truly complete clinical research management.
July 14, 2015 – ROCHESTER, NY – The latest iteration of Clinical Conductor CTMS continues the proven strategy of providing research organizations with the most in-depth features and functionality available, further distancing the application from others in the industry, which fail to provide the tools necessary for truly complete clinical research management.
The new Clinical Conductor contains a myriad of enhancements that foster more precise reporting and analysis, resulting in greater confidence in the accuracy of study and patient information, yielding greater confidence in decision making and overall business management. Updates can be seen throughout the application, with standout enhancements made to billing compliance review processes, intuitive invoicing advancements, adverse event management and reporting, forecasting, and overall system workflow efficiency. All enhancements to Clinical Conductor are aimed at meeting current and future industry needs while facilitating compliance, efficiency and profitability in conducted clinical research.
The billing compliance review enhancements in Clinical Conductor CTMS give organizations the tools they need to confidently identify charges that will be allocated to sponsors, Medicare, third-party payers and other financial entities, in a manner that is compliant with federal and state regulations. This enhanced section of Clinical Conductor gives sites in-depth billing display pages that clearly highlight important information such as procedure details, CPT codes, completion locations and more. With this comes a granular audit trail of what and when an item was reviewed, as well as who was the reviewer. Sites can also restrict access to this functionality to specific users on their team. This billing compliance review functionality also flows nicely to Clinical Conductor Enterprise users, who can review and give final approval on all items up for billing review.
The CTMS invoicing also received detailed updates that give research organizations more flexibility and greater accuracy while reviewing and generating invoices. Now, organizations can implement varying invoice frequencies within a single budget, while adhering to predetermined invoicing caps. From there, invoices and reports can be generated in real time, with all relevant invoicing data directed to the forecasting reports within Clinical Conductor CTMS for the most accurate cash and revenue projection possible.
Knowing how critical patient safety is to the industry, Clinical Conductor CTMS has received additions to the adverse event (AE/SAE) management functionality included in the system. Now, Clinical Conductor is fitted with an AE reporting wizard for more accurate and thorough reporting of AEs and SAEs. To build on this, users can now add customized notes for additional AE information, in addition to having the ability to upload any other necessary documents that pertain to an adverse event. Monitors and Sponsors can also access the real-time AE/SAE reports via Clinical Conductor portals to ensure compliance and patient safety is consistent with the study protocol.
“Underestimating the importance of precise data gathering and accurate reporting can be costly for organizations regardless of how many studies they run,” states Bio-Optronics VP and COO Jeff Markin. “The team behind Clinical Conductor provides the industry the only CTMS aimed atyielding more reliable data analysis and better decision making, with greater research profitability overall. By embracing this philosophy, we provide an invaluable tool research organizations come to rely on for years and through countless clinical trials.”
.
Behind the Buzz: Why Clinical Research Leaders Flock to SCOPE Summit
February 7th 2025In this episode, we meet with Micah Lieberman, Executive Conference Director for SCOPE Summit (Summit for Clinical Ops Executives) at Cambridge Innovation Institute. We will dive deep into the critical role of collaboration within the clinical research ecosystem. How do we bring together diverse stakeholders—sponsors, CROs, clinical trial tech innovators, suppliers, patients, sites, advocacy organizations, investors, and non-profits—to share best practices in trial design, program planning, innovation, and clinical operations? We’ll explore why it’s vital for thought leaders to step beyond their own organizations and learn from others, exchanging ideas that drive advancements in clinical research. Additionally, we’ll discuss the pivotal role of scientific conferences like SCOPE Summit in fostering these essential connections and collaborations, helping shape the future of clinical trials. Join us as we uncover how collective wisdom and cross-industry partnerships are transforming the landscape of clinical research.
SOUL Trial Shows Oral Semaglutide Significantly Reduces Cardiovascular Risk in Type 2 Diabetes
April 3rd 2025Phase III SOUL trial shows daily oral semaglutide lowers the risk of major adverse cardiovascular events in patients with type 2 diabetes and atherosclerotic cardiovascular disease or chronic kidney disease, with benefits consistent with injectable semaglutide and other GLP-1 receptor agonists.
Reaching Diverse Patient Populations With Personalized Treatment Methods
January 20th 2025Daejin Abidoye, head of solid tumors, oncology development, AbbVie, discusses a number of topics around diversity in clinical research including industry’s greatest challenges in reaching diverse patient populations, personalized treatment methods, recruitment strategies, and more.