Using the principles of Data Science, we can help pharma companies to discover powerful information from the raw data captured during the conduct of clinical trials. Our technical and functional domain experts have a broad range of experience in fulfilling a wide variety of clinical reporting requirements from different types of clients for various business needs across therapeutic areas.
What Can we Offer
Based on your business requirements, our team can develop a wide-range of reports and dashboards for:
- Grouping, Ranking and Strategic Decision Making
- Summarizing Operations and Performance KPIs
- Understanding Process Productivity and Outcomes
- Identifying Quality, Risk and Compliance Risks
Gain Insights on Clinical Data and Trial Outcomes
Business Reports
- Clinical Study Data Listings
- Lab Data Reports
- Study Database Build
- CRF Review
- Sites and Subjects Data Listings
Dashboards
- Clinical Trial Progress
- Global Subject Recruitment
- Trial Monitoring Outcomes Tracking
- Sites and Investigators Quality and Compliance
- Study Budgets and Expenditures
- Study Database Build Status
- Study Data Query and Resolution Status
News & Updates
How to Proactively Prevent Clinical Trial Protocol Deviations and Protocol Violations
Understanding the Importance of a Clinical Trial Protocol The fundamental objective of a clinical trial protocol is to provide common scientific guidance on how to conduct the clinical study in a regulatory-compliant manner and gather data that will ultimately provide answers on the safety and efficacy of the investigational medicinal product. The Guidelines for Good [...]
Food & Nutraceuticals: How Companies can Prove Health Value with Clinical Trials
What are Food and Nutraceuticals? ‘Nutraceuticals’ is a composite term of ‘nutrition’ and ‘pharmaceutical’. They are a blend of products that possess both nutritional as well as medicinal value. They are designed to improve physical health, boost immunity, and deal with stress and increase longevity. Nutraceutical products play a significant role in maintaining normal physiological [...]
Best Practices for Signal Management in Pharmacovigilance
Pharmacovigilance involves the collection, detection, assessment, and monitoring of data on Adverse Drug Reactions (ADRs) which must be evaluated to derive vital safety information. Signal detection involves monitoring the adverse reaction data for patterns that suggest new safety information. Safety signals can be detected from an extensive range of sources, such as spontaneous reports, clinical [...]