Bookshelf v8.1/8.2: What's New in This Release

What's New in This Release

What's New in Siebel Life Sciences Guide, Version 8.1/8.2

No new features have been added to this guide for this release. This guide has been updated to reflect only product name changes.

The content for Oracle's Siebel Clinical Trial Management System product has been moved to Siebel Clinical Trial Management System Guide.

NOTE: Oracle provides some of the functionality that this guide describes as part of a maintenance release. To use this functionality, you must install the required maintenance release, and perform the postinstallation configuration tasks. To complete the prerequisite installation and setup tasks, see the applicable Siebel Maintenance Release Guide on My Oracle Support

What's New in Siebel Life Sciences Guide, Version 8.1, Rev. B

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

Table 1. 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.

What's New in Siebel Life Sciences Guide, Version 8.2

Table 2 lists changes in Version 8.2 of the documentation to support release 8.2 of the software.

Table 2. What's New in Siebel Life Sciences Guide, Version 8.2
Topic	Description
About Features for Call Planning Specific to the Japanese Pharmaceutical Market	New topic. It provides an overview of new features that address regulatory restrictions in the Japanese pharmaceutical market.
Managing the PMS and Pre-Explain PMS Features	New topic. Tasks specific to Post Market Surveillance (PMS) and Pre-Explain PMS features. With PMS, users can create and track obligatory visits with hospital contacts before and after a new drug is launched.
Managing the PID Feature	New topic. Tasks specific to Product Insert Delivery (PID). With PID, users can create and track obligatory visits with hospital contacts when a package insert for a drug is modified.
Marking Package Insert Delivery and Post Market Surveillance Calls as Complete	New topic. Tasks specific to marking PMS and PID calls as complete.
Managing Accounts Contacts in Life Sciences	Enhanced functionality includes: Deleting Multiple Calls in the Accounts Contacts Call Planning Screen Switching to Reporting Mode in the Accounts Contacts Call Planning Screen Displaying Calls Created by Other Representatives
Using Signature Control for Personalized Content Delivery	New topic. It describes how to use signature control.

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