What makes us different—The Amarex Advantage

Parallel processing approach: Amarex helps save you time and money by employing a parallel processing approach. This fresh and innovative approach initiates various stages of a clinical trial (design, conduct, analyses, reporting) simultaneously rather than sequentially. We save you even more time by using the latest internet-based technology for data collection and data analysis.

Data access and review: While the study is being conducted, we provide you with data listings and data summary tables on an on-going basis, providing almost real-time access to study results. This, along with preparation and approval of a report shell early in the trial, are proven methods for reducing the time required to produce final analyses and reports.

Active involvement of Amarex principals: From the beginning to the conclusion of each project, the active involvement of Amarex principals ensures the quality, responsiveness, timeliness, and cost efficiency of our services.

Automated and standardized procedures are employed to reduce development time and cost and to ensure quality control. For example, automated checks provide rapid data cleaning, Case Report Form tracking provide constant trial status, and multiple
validation steps assure accurate results.

Written study conduct documentation, including clinical monitoring plans, data management plans, and statistical analysis plans are provided to our clients at the end of each trial. This organized compilation of study conduct and analysis documentation is an invaluable resource for potential FDA audit during the approval process.