Clinical Insights
Leverage the power of clinical data to make informed and meaningful decisions that will help your clinical studies to complete faster than you would have imagined. We help you bring clinical trial study data from multiple source systems, clean and load them into your EDC system.
Once we know your specific clinical operational and regulatory goals, we can implement a strategy in alignment to your clinical ops and regulatory affair office needs.
Track Protocol Changes
We help you efficiently track your protocol changes and perform impact analysis for your downstream processes
Streamline Clinical Documentation for Faster Submission
Whether its IND application, protocol documentation or clinical study report, we help you streamline the documentation process in alignment with regulations
Automating the information flow across the stakeholders to fast track decision making
We help you in mining information from clinical trial data and present reports that goes for faster decision making across different stakeholders associated with the study
Real time visibility
We work with your quality and regulatory team to build real time visibility of quality information across the trial operations
Visualize and empower your decision making
We help you empower your decision makings with actionable insights on quality events like deviations, adverse events, CAPAs and more
Locations
US:
39899 Balentine Drive,Suite 200
Newark, CA 94560
Phone: +1-(408) 883 - 7902
India:
Ven Business Center I, First Floor, Baner - Pashan Link Rd, Pashan, Pune, Maharashtra 411021
Phone: +91 - 20 6723 6382
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