Dash of Tech Intelligence to Clinical Trial Research Leads to Alchemy


Technology in Clinical Trial Services


About Service
Clinical Trial Data Combined With Advanced Business Intelligence Technology Will Benefit Our Customer To Save Cost And Time.
Organized Service Offering
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- The trial kick off on time
- Standardized eCRFs development is ready to map into respective SDTM domains
- Collect unambiguous and quality data from sites
- Timely receipt of external vendor/third party data
- Frequent review of Safety and Protocol end points data via BI tools
- Insight generation to Clinical Operations and CDM team on foresighted risks
- Custom solutions to handle the live integrated data of eCOA/ePRO


Quality Control (Contracted and Non-contracted)
Clinical Data Management (CDM)
- Database build, testing, and deployment
- Data entry (if needed), validation/verification
- Medical Coding
- Safety and external data reconciliation
- Site/CRA EDC training (on demand)
- EDC user/site administration
- Database lock and study closure
- Database migration/rescue from legacy systems
- Integration of EDC with other clinical applications
- SDTM/ADAM Mapping
- Study data archival
- Custom Function development (specific to RAVE)
- Custom Reporting and Visualization development
- Business Objects Reports
- Crystal Reports development
- Spotfire Business Intelligence tool
- Power BI tool
- SAS/SQL Based reporting
- Custom Scripts (specific to RAVE)


Other Services
Consulting for Clinical Trial Services
- Bespoke Solutions
- expertise
FOLLOWING ARE THE VALIDATED BESPOKE SOLUTIONS TO OUR CUSTOMERS
- Application development for Pharma/Life Science companies to manage their routine tasks digitally with less human intervention
- Advanced Technology adoption to manage the new complexities in Clinical Trial execution for a better TAT on Clinical Trial activities
- Data Aggregation and Analysis to generate insight for the future trial pipeline
- Like disease prevalence
- Potential Recruiters
- Post marketing safety assessments
- Sales feedback to initiate the R & D for molecule efficacy
Consulting service is not limited to the Clinical trial related software. This is extended to organizational
level applications developed to manage day-to-day business activities. The major highlight whereour services strengthened/utilized to multifold in last five years is integrations with EDC platforms with a wide range of Clinical applications or S/W:
- Randomization and Trial Supply Management (RTSM)
- Clinical Trial Management System (CTMS)
- Medical Imaging Systems
- Cloud Administration
- ePRO/eCOA
- Safety gateway/DB
- Targeted SDV support
- Batch Uploader




Excellence, Efficiency and Results
One of the key factors for a successful clinical study is
to have an experienced team who can confidently execute your clinical trial on time with utmost and high-quality deliverables.
- Team of industry experts and clinical professionals
- CDM “Full Service” support on all major EDC platforms
- Experienced in multiple EDC Platforms on Study Build
- Cost effective solution due to the technology/solutions
- Disaster Recovery Planning and Execution
Our focus is on utmost data quality and cost effective processes in validating the trial data. We had designed and tested the automated data validation/cleaning process keeping in mind the ease of adoption and pocket friendly to Customers. From the day we learnt Pharma industry will see a Paradigm shift in conducting trials our research involving industry experts and well qualified technology architects also began.
The result of this brainstorming and research in the Clinical Trial conduct process involving multiple functional teams leading the ParadigmIT to be in the forefront.
- Reduction of Specification review and Study build TAT
- Improved Cognitive data insights generation using Business Intelligence tools
- Reduction in data cleaning/validating TAT Improved KPI of LPLV to DBL
- Recommendation of enhancing the EDC Platform and Clinical Tools based on our Technology DNA