Bookshelf v8.1: What's New in This Release

What's New in This Release

Table 1 lists changes in Version 8.1, Rev. F of the documentation to support release 8.1.1.7 of the software.

Table 1. What's New in Siebel Life Sciences Guide, Version 8.1, Rev. F
Topic	Description
Setting Up and Configuring Clinical Study Site Visit Data Integration	New chapter. It describes how to integrate clinical study site visit data between Oracle's Siebel Clinical and a third-party application.

Table 2 lists changes in Version 8.1, Rev. E of the documentation to support release 8.1.1.6 of the software.

Table 2. What's New in Siebel Life Sciences Guide, Version 8.1, Rev. E
Topic	Description
Setting Up and Configuring Safety System Integration	New chapter. It describes how to configure Oracle's Siebel Medical for integration with a third-party safety system.

Table 3 lists changes in Version 8.1, Rev. D of the documentation to support release 8.1.1.5 of the software.

Table 3. What's New in Siebel Life Sciences Guide, Version 8.1, Rev. D
Topic	Description
Setting Up and Configuring Clinical Trial Payments Integration	New chapter. It describes how to configure Siebel Clinical for integration with a third-party payments system.

Table 4 lists changes in Version 8.1, Rev. C of the documentation to support this release of the software.

Table 4. What's New in Siebel Life Sciences Guide, Version 8.1, Rev. C
Topic	Description
Setting Up and Configuring Clinical Study Integration	New chapter. It describes how to configure Siebel Clinical for integration with a third-party clinical study application.

Table 5 lists changes in Version 8.1, Rev. B of the documentation to support release 8.1 of the software.

Table 5. What's New in Siebel Life Sciences Guide, Version 8.1, Rev. B
Topic	Description
Managing Batch Electronic Medical Device Reporting	New topic. Tasks specific to submitting Electronic Medical Device Reporting in batch mode.
Enhanced functionality with Regulatory Reporting See About Regulatory Reports	New topics include information about: Electronic Medical Device Reporting FDA Confirmations for Electronic Medical Device Reporting
Enhanced functionality Generating Regulatory Report Numbers and Submitting Reports,	Modified topic. Additional steps that must be completed to electronically submit regulatory reports to the FDA.

Table 6 lists changes in Version 8.1, Rev. A of the documentation to support release 8.1 of the software.

Table 6. What's New in Siebel Life Sciences Guide, Version 8.1 Rev. A
Topic	Description
Entering and Reviewing Data for 3500A Reports	Removed some fields for reporting adverse events on Form 3500A so that it complies with the new FDA mandate.
Service User Properties	Included a section about the Service user properties.
Siebel Pharma Business Component User Properties	Included a section about the Business Component (BC) user properties.

Table 7 lists changes in Version 8.1 of the documentation to support release 8.1 of the software.

Table 7. What's New in Siebel Life Sciences Guide, Version 8.1
Topic	Description
Table 18	Added the AxProperty: WritingGuide user property.
Recording and Submitting Contact Calls	Updated this section to include sampling allocation functionality.
Managing Pharma Samples	Updated this chapter with Sample Management and Sample Compliance functionality.
Setting Up MedEd Events	Updated procedures about allocating event costs across team members and across product lines.
Enabling Workflow Policies for LS Clinical Rollup	Added new topic about enabling workflow policies for clinical rollup.
Using Personalized Content Delivery	Added a chapter about how to use Personalized Content Delivery (PCD). PCD enables sales representatives to convey product messages to customers during face-to-face sales calls.
Configuring Personalized Content Delivery	Added a section about configuring PCD to Appendix A.
Configuring Data for Oracle Pharma Sales Analytics	Updated references from Siebel Analytics products to reflect the current Oracle Analytics product names in various places throughout the appendix.

Siebel Life Sciences Guide		Copyright © 2012, Oracle and/or its affiliates. All rights reserved. Legal Notices.