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
Including Women of Childbearing Age in Clinical Research
March 26th 2024In recognition of International Women's Month, we're featuring this recent talk between Associate Editor Miranda Schmalfuhs and Marie Teil, Global Head of UCB’s Women of Childbearing Age Program. They speak about the specific challenges women with chronic illnesses face when accessing appropriate treatment and participating in clinical trials, UCB's Women of Childbearing Age Program and it’s most successful strategies, and much more.
Using Patient Reported Outcomes in Dermatology Trials
April 25th 2024In part 3 of this video interview with ACT editor Andy Studna, Melissa Mooney, director, eCOA sales engineering, IQVIA sheds light on the unique challenges of dermatology trials and how clinical outcome assessments can be implemented in them.
Improving Engagement While Maintaining Data Integrity & Validity
March 19th 2024In recognition of Women's Health Month, we're featuring this recent talk between Associate Editor Miranda Schmalfuhs and uMotif's Chief Product Officer, Julia Lakeland, discuss new technologies improving patient engagement and reducing the emotional and logistical burdens of participation, ethical considerations that should be addressed when implementing those technologies, while ensuring patient privacy, and much more.
