10 Reasons

Why You Need Siebel Clinical Trial Management System

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

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Centralized Investigator Database

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

8 7

Transparent Financial Tracking

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

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
Ability to Integrate
Streamline processes even further through automated interfaces with other clinical systems.

Increased Recruitment Visibility

Track subject enrollment across studies and clinical programs against planned targets.

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Greater Compliance

Adhere to regulatory requirements and guidelines through user access controls, enforced processes, and behind-the-scenes tracking, such as audit trails.

Robust Reporting

Answer questions quickly and easily with ad hoc and canned reports that query one centralized database.

Informed Decision-Making

Identify trends and inconsistencies across investigators, trials, and business units.

Scalable Growth

Increase the number and size of the trials you manage with fewer additional resources.