 |
Scott Cooley replied: (6th Sep, 2009)
Electronic CRFs have progressively become the standard for clinical trial conduct. Both from the perspective of the sponsor and the investigator they are easier to manage, provide immediate feedback for errors, provide for continuous assessment trial progress, enrollment, assistance to sites and shortened closure at study end. A good eCRF system should be able to handle both data entry by investigator and staff as well as subjects, and transfer of data from external sources such as lab, IVR, etc. There's a good chance you won't want to ever return to paper. |
delete
|
