Clinical Development Services

We manage clinical trials from Phase I safety studies through Phase IV post-marketing surveillance, handling the logistics so you can focus on the science.

Overview

Running a clinical trial means coordinating dozens of moving parts - sites, patients, monitors, labs, data managers, and regulators. We've managed trials ranging from 20-subject Phase I studies to 500-patient Phase III programs across multiple countries. Our team knows how to keep trials on schedule and on budget.

What We Do

Phase I dose-escalation studies using 3+3 designs or modified Fibonacci schemes

Multi-center Phase II and III trials with site selection and feasibility assessments

Clinical monitoring visits to verify informed consent, source documents, and protocol compliance

Managing investigational product supply chains and temperature-controlled storage

Coordinating with central labs, imaging core facilities, and independent review committees

Why Work With Us

Our monitors average 8+ years of clinical research experience

We use risk-based monitoring strategies to focus resources where they matter most

Proven track record managing trials that led to successful regulatory approvals

Related Services

Clinical Data Management

EDC systems and data quality control

Pharmacovigilance

Safety monitoring and adverse event reporting

Project Management

Timeline and budget coordination

Central Laboratory

Clinical lab testing and sample management

Ready to Get Started?

Let's discuss how we can support your clinical development services needs.