Clinical Research Services
Comprehensive clinical trial solutions covering Phase I–IV studies, safety and efficacy assessments, regulatory support, and post-marketing surveillance designed to accelerate development timelines with precision and compliance.
Full-Spectrum Clinical Research. Focused on Your Success.
BioAgile delivers integrated clinical research solutions across the development lifecycle from first-in-human to post-marketing. Our services span study design, regulatory submissions, site management, data collection, and analysis ensuring every trial is ethical, efficient, and ready for global markets.
We Provide the Best Service for you
Our Practice Areas and Expertise
Safety Assessment
Comprehensive safety profiling through preclinical and clinical studies—covering toxicity monitoring, adverse event evaluation, dose-ranging, and long-term risk detection—to ensure product…
Efficacy Evaluation
Rigorous clinical and outcome-based studies designed to measure therapeutic benefits across populations—powered by statistically driven endpoints, optimized protocol design, and…
Label Claims Substantiation
Evidence-driven support for product claims—covering nutrient content, structure/function, health, and cosmetic assertions. We ensure each label statement is backed by…
Clinical Quality Assurance
Proactive auditing, SOP compliance, and risk-based monitoring—ensuring GCP-aligned processes and uncompromised study integrity at every stage.
Clinical Data Management
Accurate, timely, and regulatory-compliant data handling—from CRF design to database lock—ensuring high-quality datasets for confident decision-making.
Biostatistics
Robust statistical planning, analysis, and reporting—ensuring data integrity, regulatory compliance, and scientifically sound conclusions across all study phases.
Regulatory Support
Strategic guidance and submission expertise across global regulatory frameworks—ensuring timely approvals, compliant documentation, and seamless stakeholder alignment.
Clinical Trials (Phase I to Phase IV)
End-to-end execution of Phase I–IV trials with scientific rigor, regulatory alignment, and operational excellence—ensuring reliable outcomes across diverse therapeutic areas.
Medical Writing
Clear, compliant, and publication-ready documents—from clinical study protocols to regulatory dossiers—crafted to meet global standards and accelerate submissions.