Clinical Trial Services
Accelerate Your Clinical Trials in India
eteraflex delivers end-to-end clinical trial services across every phase of drug development — from protocol design to final regulatory submission. With 240+ validated research sites, experienced teams, and a proven 4-week database lock, we help global pharmaceutical and biotech companies accelerate drug development while maintaining world-class compliance and data integrity.
Clinical Trial Services for Every Phase
eterflex provides a unified framework for clinical operations, combining scientific expertise with data-driven technology.
Our trials cover Phase I to Phase IV programs and span major therapeutic areas such as oncology, immunology, rare diseases, cardiovascular, neurology, and pediatrics.
Our Clinical Trial Capabilities
Phase I–IV Pharmaceutical Programs:
Our India-based clinical programs deliver full-cycle drug development support through
Oncology and Immunology:
Specialized KOL networks and biologic trials at premier cancer centers.
Rare and Complex Diseases:
Nationwide reach to access targeted patient populations.
Cardiovascular and Neurolo
Conducted at tier-1 specialty hospitals with advanced diagnostics.
Pediatric and Precision Medicine Studies
Focused on specialized children’s research facilities and genetic-based therapies.
Our services span Phases I–IV, covering everything from protocol design and site management to patient recruitment, data management, and regulatory submission.
How We Deliver
EteraFlex ensures seamless trial execution through a structured and transparent operations framework:
- Dedicated Project Management: End-to-end oversight with clear milestones and progress tracking.
- Adaptive Resource Planning: Smart allocation and forecasting for on-time study completion.
- Site & Investigator Management: Continuous performance optimization across 240+ validated centers.
- Patient Recruitment & Retention: Strategic enrollment planning with predictive analytics.
- Regulatory Coordination: Ethics submissions and clearance achieved in 4–5 weeks on average.
Our integrated approach enables faster timelines and consistent study quality, across both local and multinational projects.
Technology & Quality
ClintrialX Data Platform — Built for Speed and Compliance
EteraFlex leverages its proprietary ClintrialX platform to simplify and accelerate every data-driven process.
Platform Advantages
- Database lock achieved in just 4 weeks
- Automated QA cycles reducing manual review by 65%
- Real-time monitoring and predictive issue tracking
- FDA, EMA, and CDSCO-compliant data packages
Quality & Compliance Framework
- Risk-Based Monitoring: Centralized oversight and continuous risk detection.
- Automated CAPA Systems: Root-cause analysis and fast issue resolution.
- Regulatory Readiness: Proven 100% inspection pass rate on all completed trials.
- Continuous Improvement: Ongoing audit tracking and compliance documentation.
A Trusted Clinical Network Across India
Our research network extends across government teaching hospitals, corporate hospital chains, and specialty medical centers — providing broad patient access and reliable enrollment results. Every site within our 240+ center network is pre-qualified for infrastructure, compliance, and performance consistency.
Robust Clinical Infrastructure
Advanced diagnostic and laboratory support
High-Performance Sites
Specialty centers with high enrollment success rates
Standardized Quality Framework
Standardized data and quality frameworks across institutions
