What's the deal with Content Plan Templates?
This tool can update the order of existing content plan templates in an environment
What is the Content Plan Template Reordering tool?
As of this release, our template vault supports US eCTD 4.0 Publishing & Validation v1.8
What is 26R1?
This Application is not required for Publishing Customers
What is Registrations?
Using this spreadsheet application often times misrepresents foreign characters such as 木 or 漢字
What is Excel?
For most customers, this state is where you click the action 'Submit to Gateway'
This Market introduces separate CPI's in Module 4 and Module 5 as part of their specifications
What is China?
Before running the injectifier, ensure you put in a product support ticket to do the following
What is Enabling Publishing Application?
Check your SOW! This offering (managed by Kerry Shallis) may be offered as part of your Publishing project
What is Publishing eLearning?
Using this tool is now considered our 'best practice' for both comparing and build loader sheets for reference data
What is VEM Next Gen?
When configuring a gateway profile, the digital Sponsor Certificate uploaded by an administrator must be in this specific file format
What is PKCS12 (or .pfx / .p12)?
If your customer has an older vault this field may cause some fits when trying to load in content plan templates. If there are gaps, it would be worth your time to map these with your customer
What is Doc Type Details? (also type/subtype/classification)
What is the Ready for Publishing field?
This Feature is required for any future Publishing Customer
What is Submission Wizard?
This object record which is referenced by the region has a circular dependency and should be loaded twice, once without Health Authorties, and once with Health Authorities once Health Authorities have been loaded
What is the Country record?
This number is the expected number of acknowledgements back from the FDA for a test submission in your SBX/VAL environment
What is two?
This is the 'Correct Order' when Loading in Content Plan Related object records
What is Content Plans (w/o Parent), Content Plans (w/ Parent), Content Plan Items, Content Plan Template Constraints?
This object maintained by product can be leveraged to create specific Application templates by removing configuration that is not relevant to a specific Application
What is the Template Manifest?
Our job as consultants is to teach organizations how to use Veeva Publishing, not how to successfully publish a Submission. Its important that an organization has this role defined before starting a project.
Who is a Publisher?
If updating existing customers Submission Joins from a custom object type to a standard object type, this field must be populated in order for the system to take action?
What is the Application Source field?
If an FDA submission receives a technical rejection, an administrator can run this record action on the related Dossier Details record in the "Transmission Successful" state to unlock the sequence and allow for a resubmission
What is the Prepare Resubmission action?
These four fields are not available to be referenced within a token on your Content Plan/Content Plan Item Templates
What is Long Text, Rich Text, Formula Fields, and fields referencing the User object?
While this daily batch cleanup job is designed to automatically remove imported files after a submission structure is deleted, Veeva explicitly recommends against enabling it if the organization you are working with manually creates documents of the Submissions Archive (archive__v) type, as Vault will delete them anyway even if their Application and Submission fields are populated
What is the Submissions Archive Delete Orphaned Files job?
This workstream should be started as early as possible as it's related to a core functionality of Publishing and requires the customer to work with certain Health Authorities
What is the ESG (Electronic Submissions Gateway) workstream
This field on the controlled vocabulary object references other CV's and should be considered when loading in standard Controlled Vocabularies into a customer's environment
What is CV Value Filter?
As of July 10th, 2026, the US FDA has communicated that this item for the FDA TEST environment should be replaced by this item currently being used in the FDA Production Environment.
What is a Gateway Certificate?