| 摘要 |
The present invention implements a computer-based system and procedure for the efficient and effective preparation for conducting at least one clinical trial. The various methods are deployed using a Software As A Service (“SaaS”) platform, allowing access to the system by all relevant participants. Each authorized participant in a proposed clinical trial may access a customized and customizable view of the data necessary to gain approval for conducting a clinical trial and interact with the other participants electronically, prior to initiation of a clinical trial or study. The various documents needed for the clinical trial or study, as well as the various compliance documents needed to satisfy regulatory agencies are all available for review via the Internet. By utilizing present invention, greater protection is offered for the human subjects of the clinical trials. Further, the invention offers increased productivity for sponsors, investigators, and the study participants. |
