| 摘要 |
A system for automated management of a clinical trial for pharmaceutical, biomedical, and medical device development that facilitates pharmaceutical research and reporting, including at least one site server 222, at least one computing device 218 configured to collect primary clinical trial data, and an authorized user accessible computing device 234. The central server 232 is configured to receive the primary clinical trial data from each site server 222, to store the primary clinical trial data, to create secondary clinical trial data based on the primary clinical trial data, and to transmit the primary and secondary clinical trial data to the authorized user accessible computing device 234. Also provided is a method for automatically managing a clinical trial for pharmaceutical, biomedical, and medical device development in order to facilitate pharmaceutical research and reporting, which further includes a computer readable signal containing a set of instructions to perform a corresponding method. |
