Once preclinical testing is complete, a new drug candidate, biologic, or medical device begins the lengthy and costly human clinical trial process, with the goal of ensuring a safe and effective therapeutic treatment. The success of this process—and the medical and commercial success of the treatment—is determined by the ability of the research sponsor to navigate through the process safely and speedily, collecting scientific and medical data, analyzing it and reporting it.
Innovative process design, technology and services streamline clinical trials by providing early visibility to reliable clinical data. Our products span the clinical research process and, through integrations with other applications, can serve as the backbone of the eClinical process.
Medidata's innovative products address these activities in the clinical trial process: