Clinical Research Services
Our integrated clinical research services spread from bioequivalence studies to phase I-IV clinical trials.
Clinical Operations
Clinical Data Management
Data Management
Biostatistics
Medical Writing
Clinical Pharmacology
Clinical Trial Supplies & Logistics
We collaborate in the development of new medical treatments and technologies to advance health science and accelerate patient access. Each day, we’re driven to make a meaningful impact by providing comprehensive services — from trial design, planning, and site feasibility to regulatory submission, project management, monitoring, quality control, and auditing.
Our integrated clinical research services spread from bioequivalence studies to phase I-IV clinical trials
Study Operations
Oversight and execution of clinical trials, from site selection to study close-out.
Data Management & Quality
Collection, cleaning, and validation of clinical trial data to ensure accuracy and reliability.
Statistical Analysis
Design, analysis, and interpretation of clinical trial data using rigorous statistical methods.
Scientific & Regulatory Writing
Preparation of clinical documents including protocols, study reports, and regulatory submissions.
Pharmacology & Drug Safety
Expertise in drug absorption, metabolism, and interactions to support trial design and safety.
Trial Supply & Logistics
End-to-end management of investigational product supply, storage, and distribution.
Through our FSP model, we provide dedicated local professionals who bring specialized expertise and seamlessly operate as an extension of your organization.