What we do

We work for, and have preferred supplier status with, some of the world’s leading pharmaceutical and biotechnology companies. Trials are conducted in accordance with ICH GCP guidelines, all applicable regulations and legislation, and any requirements specific to the project. Our highly qualified team will:

• Rapidly identify sites which best meet your needs, drawing on our extensive database of more than 2000 clinical research centers throughout the region
• Organize the entire study documentation workflow, including preparation, translation, review and submission
• Plan and manage every aspect of the trial, from start-up to completion
• Provide full monitoring, site management, financial control and logistical support