Our Services
Whether you’re launching a new study or preparing for regulatory review, we’re here to guide you with trusted, data-driven insight
Clinical Trial Design
We support clinical protocol development, sample size calculation, and creation of key planning documents, including SAPs, PSAPs, LOAs, and shell templates
Programming & Statistical Analysis
End-to-end data programming and statistical analysis, ensuring accuracy, efficiency, and compliance for clinical trial data
Regulatory Analysis & Reports
Preparation of clinical study reports (CSRs), Summary of Clinical Safety (SCS), and Integrated Summary of Safety (ISS) for global regulatory submissions.
Presentations & Scientific Training
Custom presentations and seminars on clinical trial design, statistical methods, integrated analyses, and regulatory topics—tailored to your team.