eShowcase
Tools for Clinical Trials Professionals
Software enables on-demand report generation from preclinical to manufacturing
iAdvantage (Cary, NC) just launched a reporting generator called ePublisher, an offshoot of the company's eStudy management solution. The standalone software, which is Web-based, enables users in life science fields the ability to design templates and generate reports on-demand. ePublisher is compatible with familiar word processing and spreadsheet software, including Word and Excel.
Available formatting options include single data points, text, tables, and images. The software can pull data from Oracle and Sequel databases simultaneously into the same report. Users point ePublisher to the data source, select the data set of interest and the desired report template, and click on "generate report."
Its manufacturer says that ePublisher reduces report generation from weeks to months, with applications from development and preclinical, including toxicology, safety, and efficacy, through to clinical and throughout the manufacturing process.
ePublisher
iAdvantage, (919) 469-3888, www.iadvantagesoftware.com
Manage recruitment from investigative site selection through patient retention
BBK Healthcare, Inc. (Newton, MA) recently released the latest version of its TrialCentralNet enrollment data management software package with enhanced functionalities. This version offers users more customization options and instant data generation. With TrialCentralNet 4.0, all key parties, from sponsors, investigative site staff, clinical research associates, country study managers, and patient recruitment professionals, have 24/7 access to clinical study enrollment data. TrialCentralNet is a secure, pass-word-protected software tool.
The manufacturer says that with TrialCentralNet, users can integrate data from many sources and quickly generate reports, plus they can customize view for individuals or groups in any language. The software package functions as a document repository for all study-related tools in a secure, regulatory-compliant "patient manager" database. The software also offers scheduling and screening functionalities.
TrialCentralNet 4.0
BBK Healthcare, Inc., (617) 630-4477, www.bbkhealthcare.com
Clinical data repository tool gives life science professionals a leg up on regulatory compliance
Oracle (Redwood Shores, CA) has unveiled a solution for bringing together clinical data from multiple sources and storing it for regulatory compliance applications. Oracle Clinical Data Repository is designed to help life science companies manage all aspects of central data repository integration, from data access to transformation to persistence and distribution.
The product is aligned with current efforts to standardize clinical data, such as those underway by CDISC. According to Oracle, the solution will provide organizations with a controlled, structured environment in which to build and store data in a ready-to-submit format. All data objects in Oracle Clinical Data Repository are fully audited and version controlled. Designed to help companies simplify data management tasks, the tools enable researchers to focus on data interpretation instead of report creation.
Oracle Clinical Data Repository
Oracle, (650) 506-7000, www.oracle.com
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.
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.
