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FAQ For Oracle Quality Application for Setup, Charts and Reports, and General Questons (Doc ID 395807.1)

Last updated on APRIL 24, 2018

Applies to:

Oracle Quality - Version 11.5.2 to 11.5.10.0 [Release 11.5]
Information in this document applies to any platform.
***Checked for relevance on 07-Aug-2012***

Purpose

This FAQ was produced to address questions and concerns regarding the Oracle Quality Application. The questions in this FAQ are categorized by Quality Topics, and are updated and kept current. 

Questions and Answers

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In this Document
Purpose
Questions and Answers
 .
 GENERAL 
 Why do records remain in a completed status in the table after a successful quality import?
 Can you limit what actions are available by the user?
 Does Oracle Discrete Manufacturing now have electronic records and signatures that help medical device customers to comply with FDA Regulations?
 Which Profile Option should be enabled to set up Electronic Records and Signatures?
 Is there a way to make QA validate to ensure that there was a move order already created for item/serial number combination?
 Is there a need to have a separate 'Criteria' created for each discrete "Skip Lot" / "Sampling Plan" combination?
 Why is there a performance issue when the update quality collection plan folder is open and collection element is selected?
 Why doesn't e-records and e-signature work for nonconformance creation in the Quality Workbench?
 Why does the quality actions program(QLTACTWB)fail with "One or more of our actions failed. Please check the Action Log form for details"?
 How exactly statuses of the CARs(and NCRs, NCRs dispositions as well) are being changed (PENDING -> APPROVED or NO APPROVAL REQUIRED etc)during their eSignature approval?
 How does one setup Nonconformance to transfer to MRB
 Why results entered from the Receiving Inspection are not in the View Quality Results window?
 Why in Oracle Quality QA_SPECS_PUB, public API does not allow user to populate attribute columns through create_specification procedure?
 .
 SETUP/HOW TO
 How do I perform a basic setup to achieve Skip Lot Inspection functionality in Receiving Quality Inspection?
 How do I Setup Parent/Child And Non-Conformance?
 How do I Change the Page Settings Used in Quality Results ReportWriter?
 Where can I find a document titled "A Guide to Oracle Quality An Oracle White Paper"?
 Oracle Quality Release 11i - Purchasing Data Collection Overview
 Implementing Audits Using Oracle Quality
 Where can I learn more about Non Conformance and Disposition Management Using Oracle Quality Solution Templates?
 How do I Implement E-Records and E-Signatures (11.5.10) in Oracle Quality?
 What is Oracle Integrated Quality Management Solution for Corrective and Preventive Actions?
 Where can I learn more about Oracle Quality Parent Child Collection Plans?
 How do I Setup eMail in Quality Module?
 Why when creating a collection plan using template scrap reject an error happens indicating: You must add From/To Operation Sequence to the collection plan and enable it before you can add From/To Intraoperation Step?
 Why when using Mobile Quality User for entering the quality results using MSCA form does it error on the collection element LOV with Unsuccessful Row construction?
 How to migrate the collection plan from instance to an other instance?
 In the Skip lot process setup, skipping parameters tab can the number of rounds and the time span parameters be set together? So if the data setup is such that the inspection frequency of 1 in 2 is applicable for 5 rounds for a time span of 60 days, does it mean that the skip lot plan will not move to the next sequence if the 5 rounds are not done within 60 days?
 .
 CHARTS AND REPORTS
 Where can I find a document titled "A Guide to Oracle Quality Reports An Oracle White Paper"?
 How do I Change the Page Settings Used in Quality Results ReportWriter?
 Are there Collective Action Request canned reports available with the Quality Module?
References

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