eClinical Software: August 2009
The latest eclinical software in the clinical trials industry.
Planning and Analyzing Patient Recruitment
New module broadens planning and forecasting at site level
KMR Group (Chicago) has added a new module in its Enrollment Metrix Application called SiteView. SiteView offers users the ability to examine enrollment KPIs derived from site level data. The new module allows users to anticipate the expected number of patients to be recruited from any given site as well as the time it takes any given site to complete recruitment.
SiteView increases site knowledge
SiteView joins with the TrialView module, which both access KMR Group's industry data, which includes disease, phase, and geography obtained from over 100,000 sites from recently completed trials in the biopharmaceutical arena.
KMR Group, (312) 795-0400, http://kmrgroup.com
Randomization/Trial Supply Management
New reporting solution addresses timeline/supply in global trials
Perceptive Informatics (Boston) announced its new reporting solution as part of its ClinPhone Randomization and Trial Supply Management (RTSM) technologies, which offer validated randomization methods, automated inventory control, dispensing and titration management, and emergency code break capabilities.
Perceptive RTSM gains reporting tool
The reporting solution features a Universal Report Suite to monitor clinical trial management performance, RTSM Dashboard with trending and forecasting functions, and a Self-Service Module with customizable search criteria for in-depth data analysis.
Perceptive Informatics, (781) 487-9900, www.perceptive.com
Enhancements Address Diaries and Interactivity
Design tool offers added function and flexibility for clinical trials
CRF Health (Lansdale, PA) announces TrialMax 4.0, which extends its ePRO software suite function. The TrialMax eDiary design tool allows real-time development between study teams and trial sponsors. In addition, TrialMax 4.0 includes automated email notification and messaging, enhanced user account and password management, configurable data exports in a variety of output formats, report content export to Microsoft Excel, enhanced report printing, and configurable patient status icons.
Introducing TrialMax 4.0
TrialMax 4.0 has also been updated with new user interface graphics and the ability to embed links in study reports.
CRF Health, (267) 498-2300, www.crfhealth.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.
Regulatory Compliance With eCOAs
April 26th 2024In the fourth and final part of this video interview with ACT editor Andy Studna, Melissa Mooney, director, eCOA sales engineering, IQVIA discusses how the regulatory stance on electronic clinical outcome assessments has changed over the years and what it could look like in the future.
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.
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.
