XTrials^® Research Services is a full-service contract research organization with international resources dedicated to the planning, execution, and analysis of phase I through Phase IV clinical trials for drugs, biologics, and medical devices.

We have been in the clinical services business for over 20 years supporting a wide range of therapeutic development and clinical operations requirements. Our central focus is on reducing the time, risk, and cost of conducting clinical programs while ensuring the highest levels of clinical practice, data integrity, and customer satisfaction. We have been very effective in achieving these objectives with agile combinations of expert talent, quality procedures, and multi-national study sites efficiently managed and coordinated via our web-based Xtrials eClinical technology.

XTrials^® Efficiency is built upon the operational backbone and collaborative workgroup environment provided by our integrated web-based eClinical platform. This technology enables our project managers to closely monitor all dimensions of study progress from multi-national enrollment accruals to disbursements, site monitoring, and database locking performance in a single, integrated, protocol-specific, workgroup environment.

XTrials^® core competencies are in protocol development, product registration, site selection and negotiation, IRB/IEC correspondence, project managements, medical and site monitoring, eClinical deployments, data managements coordination, database integration, safety monitoring and reporting, biostatistics, medical writing, and regulatory submissions. In all of these our team members are intent on harnessing both the power of global standardization and the agility and cost-effectiveness of local expertise, to bring your clinical projects in On Time, On Target, and On Budget.