Phase I - Iia Clinical Trials Overview
Scientific expertise. Regulatory acumen.
inVentiv Health Clinical conducts Phase I-IIa clinical trials quickly and efficiently at its dedicated 22,000 square foot clinical facility comprising more than 200 beds in four independent units. An extensive database and relationships with leading hospitals ensures rapid recruitment of study participants for a wide variety of trials.
In addition to a staff of eight physicians and a dedicated project manager for each study, we deploy a team of experts, including specialists in quality assurance, and scientific and regulatory affairs, to custom fit a program to your specific needs. Accordingly, advanced equipment, skilled staff, meticulous material handling, and timely reporting of our bioanalytical laboratories ensure the smooth completion of projects.
Our departments and business processes, including data processing and report writing, comply with current GCP and GLP standards, while an independent quality-assurance unit validates study data and reports, providing the basis for our exceptional regulatory success. With a full range of services from study design to submission, inVentiv Health Clinical provides everything you need to efficiently conduct your study.
Experienced, on-site physicians and medical professionals are available to ensure the safety of our participants. While many clinical studies may require a period of confinement in order to control elements of the study, semi-private rooms are available.
If you are interested in participating in a clinical study, we have opportunities for healthy volunteers and individuals who may have special conditions. Each clinical study has specific volunteer criteria that must be met in order to participate. For more information about available studies, click here.