10 Reasons Why You Need Siebel Clinical
10Reasons 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. Centralized Investigator Database Store past, present, and future investigator information in a central location that can be queried during site selection. 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. 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. 4 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. 1 Scalable Growth Increase the number and size of the trials you manage with fewer additional resources. ABIOPHARM systemš Gold ORACLE Partner Partner with an Expert www.biopharm.com [email protected] +1 877 654 0033 (US) +44 (0) 1865 910200 (UK) 2. 10Reasons 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. Centralized Investigator Database Store past, present, and future investigator information in a central location that can be queried during site selection. 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. 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. 4 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. 1 Scalable Growth Increase the number and size of the trials you manage with fewer additional resources. ABIOPHARM systemš Gold ORACLE Partner Partner with an Expert www.biopharm.com [email protected] +1 877 654 0033 (US) +44 (0) 1865 910200 (UK) 2.
10 Reasons Why You Need Siebel Clinical
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