Acceliant, the global leader in eClinical trial management solutions, today unveiled Acceliant 7.0.2, the new version of its eClinical solution. Acceliant 7.0.2 is powered by Study Data Tabulation Module (SDTM) and has new upgrades on randomization, multi-trial management and an improved mobile app user interface. With the new release, Acceliant significantly improves the eClinical trial solutions offerings by focusing on better user experience and providing a one-stop destination for global compliance standards.
Speaking on the release, Vivek Gupta, Worldwide VP at Acceliant, said, “The latest release strengthens our eClinical platform, enabling our clients to streamline the way they organize the clinical trial data across pharma, medical devices and CROs. With the CDISC SDTM capability, Acceliant users can streamline their submissions, speed up the regulatory review and approval process. A seamless collaborative platform with high quality standards will certainly drive the client satisfaction,” he added.
Following is the summary of the new features in Acceliant 7.0.2:
- SDTM: Post FDA mandate, all clinical trial data submissions made to FDA on or after December 2017 must be compliant with SDTM export. The SDTM capability of Acceliant speeds up the drug approvals for clients as they need not rely on other platforms.
- Randomization: The module enables sponsors to randomize the study participant to a treatment group or control group and eliminates dependencies on other systems.
- Multi-trial management: The upgrade facilitates a single sign on capability, intuitive dashboard, trial progress tracker and automatic trial data backup.
- Mobile App: Acceliant's mobile-first clinical trial data app, available on iTunes and Google Play app stores, aggregates clinical data at the point of capture across multiple sites and provides a consolidated view for review and analysis of data.
Acceliant provides real time, integrated clinical trial solutions for life sciences, CROs and pharma tools and expertise to take intelligent and smarter decisions. Its eClinical Suite allows users to build studies, design electronic case report forms (eCRFs), capture data through multiple sources (EDC), capture data directly from patients (ePRO), and manage other clinical data management functions.