What’s New > Windchill > 13.0.2.0 > Windchill Quality Management Solutions > Enhancements to Regulatory Submissions (Med Device)
Enhancements to Regulatory Submissions (Med Device)
Windchill 13.0.2.0
Description
Windchill now provides the ability to view acknowledgement messages for a regulatory submission in the Acknowledgement Messages table on the information page of the regulatory submission. You can configure this table on a native workflow task template.
The Regulatory Submission Type attribute allows you to define the type of regulatory submission that you want to create for a type of Customer Experience Regulatory Report Decision.
You can specify customer experience as the subject of a regulatory submission.
The Related Tasks table is enhanced to display tasks for the regulatory submissions.
The Regulatory Submission Summary table in the customer experience information page displays all the regulatory submissions with customer experiences or its regulatory report decisions assigned as the subject. It is visible only to the users in specific roles and those who are members of the View CEM Regulatory Submissions license profile.
The part information page has been enhanced to add the Regulatory tab. This tab contains the UDIs and Regulatory Submission Summary tables. The Regulatory Submission Summary table displays all the regulatory submissions in which the current part version or any predecessor versions are assigned as the subject. It is visible only to the users in specific roles and those who are members of the View Part Regulatory Submissions license profile.
You can use the samples of the latest workflows as a best practice to build your workflows.
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