Clinical trials differ in their importance and positioning of a study drug. As a result, unique configurations are necessary for registration trials (phases I-III) vs phase IV trials, including phamacovigilance trials, patient registries and observation trials.

Clinical Trials Data Center has an extensive library of study templates optimized for different study types but all share the intuitive, easy-to-use user interface. Our Patient Registry solutions offers "hands-off" data management where sites can 'deposit' data under the guidance of the on-line validation module.

Prospective controlled clinical trials are configured to support "Active Management" of the study and study data, delivering unparalleled, real-time support to all users. For example, this configuration of edc^pro supports:

• On-line / real-time randomization
• Patient scheduling & e-mail notification
• Direct access / link to all urgent tasks requiring completion
• Controlled workflow to ensure time completion, review, SDV, etc. of study data