Clinical Programming & Data Science
Making evidence-based decisions is critical to the success or failure of your study. At Allucent, our experienced data scientists and clinical programmers, along with the best technology, support your specific study needs. Our experts delve deep into your data to provide you with crucial insights, enabling decisive actions to be taken when needed.
The high quality of our data springs from our strong partnerships with technology vendors and our careful selection of cloud-based EDC (electronic data capture) systems powered by best-in-class technology. Allucent offers special insights and analytics reports that support the aggregate review of key safety and efficacy trends during the conduct of a study.
On-Demand Reporting and Insights
Combining our clinical data management services with industry-leading technology, we give you on-time, on-demand clinical data reporting and in-depth insight into your trial.
You will have 24/7 access to the systems where you can utilize advanced data integration and dynamic dashboards to see the status of your trial.
Valuable Report Format
The concise and ready-to-present format of our insights and analytic reports will help “sponsor” to present important trend data to their internal management teams, board of directors and/or investors. In addition, the reports can be used to generate abstracts, posters or oral presentations at scientific conferences.
Unique Patient Profile Reports
Our patient profile reports summarize current study data including safety, biomarker read-outs and preliminary efficacy trends (if applicable).
This will aid in decision-making for SRCs, protocol amendments, decisions on consecutive study designs, future development plans, among other important choices.
CDISC Standards
We maintain a global library of data standards according to CDISC requirements, industry standards, and best practices. We streamline processes from database design to analytic dashboard setup, and generation of SDTM/ADaM datasets, emphasizing quality, time savings, and cost efficiencies.
Insights and Analytics: Operational Metrics
- Customized metric reports
- Study metrics for close oversight & monitoring
(e.g. DRC/IDMC meetings, interim review of data) - Support Project Team/Sponsor meetings
- Early identification & timely intervention on issues
- Site performance and/or data-related issues
- Data quality and trend analysis
- Protocol non-compliance
Allucent’s insights and analytics reporting is provided at regular intervals during the trial to be used for the thorough review of data. The reports are to be seen as snapshots of the data while the trial is ongoing. They summarize current trial data including safety, biomarker read-outs, and preliminary efficacy trends.
This will aid in decision-making for DMCs/DSMBs/SRCs, protocol amendments, decisions on consecutive study designs, and future development plans, among others.
Our team has extensive experience with a broad range of electronic data capture (EDC) systems.
We carefully select cloud-based EDC systems for their user-friendly interface, additional modular options, real-time data capture, and reporting and information dashboards. All of our EDC systems are regulatory and 21 CFR Part 11–compliant.
Our clinical data management team will assist you in making the right decision based on your study-specific requirements and preferences. While we often recommend using an in-house preferred EDC platform, our team can also support the management and execution of your trial if you choose an alternative.
Allucent’s EDC Systems Expertise
Powered by best-in-class technology, Allucent is certified to build EDC systems in Merative Zelta, Medidata RAVE, and Veeva CDMS.
Our team supports:
- Merative Zelta (previously IBM Clinical Development)
- Medidata RAVE
- Veeva CDMS
- Sponsor-requested platforms
“We’re particularly enthusiastic about advancements with Artificial Intelligence (AI) and its practical applications in day-to-day activities. We emphasize leveraging AI to enhance quality, streamline workloads, and improve efficiency.”
Stephen Apps
Senior Director, Global Head of Clinical Programming
