Top 10 Reasons Why You Need a Clinical Trial Management System

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Top 10 Reasons Why You Need a Clinical Trial Management System Powered By Docstoc
					   10 Reasons
         Why You Need
       Siebel Clinical Trial
       Management System

   10                                  Simpler Maintenance
                                       Maintain one commercial system, usually with
                                       support from the vendor, rather than multiple
                                       spreadsheets and/or home-grown databases.




                       9                            Centralized Investigator Database
                                                    Store past, present, and future investigator information
                                                    in a central location that can be queried during site selection.




                                    8                            Transparent Financial Tracking
                                                                 Monitor planned costs vs. actual spend vs. outstanding
                                                                 balances for investigators, sites, sponsors, and vendors.




                                                    7                          Streamlined Document Tracking
                                                                               Create standardized lists of documents to be collected over
                                                                               the course of various types of trials, and track standardized
                                                                               dates and other information against those lists.




                                                               6                             Increased Recruitment Visibility
                                                                                             Track subject enrollment across studies and
                                                                                             clinical programs against planned targets.




Ability to Integrate
Streamline processes even further through
automated interfaces with other clinical systems.
                                                                             5
               Greater Compliance
               Adhere to regulatory requirements and guidelines
               through user access controls, enforced processes,
               and behind-the-scenes tracking, such as audit trails.
                                                                                            4
                               Robust Reporting
                               Answer questions quickly and easily with ad hoc and
                               canned reports that query one centralized database.
                                                                                                         3
                                               Informed Decision-Making
                                               Identify trends and inconsistencies across
                                               investigators, trials, and business units.
                                                                                                                       2
                                                               Scalable Growth
                                                               Increase the number and size of the trials you
                                                               manage with fewer additional resources.
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posted:1/23/2013
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