Create a Submission to report a case to a regulatory agency.
Note: Depending on your Admin’s configuration, object, field, and section labels, lifecycle states, and workflows may differ from the general information on this page. Refer to your organization’s business processes for guidance.
Creating Submissions
Submissions can be created automatically during Case workflows, or manually.
The Submission workflow depends on your Admin’s configuration. By default, after a Submission is created, Vault Safety assigns a task to users in the Distribution Manager role to review and approve the Transmission and Individual Case Safety Report (ICSR) document before transmitting the Submission.
Prerequisites
- Your Admin must have configured the Transmission Profile and AS2 Connection for the destination agency.
- To automatically generate Submissions, your Admin must configure the appropriate reporting rules.
- You must have permissions to manage Transmission object records. Typically, these permissions are reserved for Distribution Manager users.
- To submit Clinical Trial Cases with the Spontaneous Report Type in EMA E2B(R3) reports, your Admin must enable EMA Clinical Trial Submissions: Non-Study Suspect Products.
Automatic Creation
Vault Safety automatically creates Submission records when the Evaluate Reporting Obligations action runs on the Case. By default, when a Case enters the Approved state, Vault creates any necessary Submissions.
Note: When Submissions are generated for a Domestic Case, Vault automatically links any Localized Cases for countries within the reporting jurisdiction.
The Submissions that Vault Safety generates depends on individual Case criteria and the active Submission Rules in your Vault.
Regenerate Automatically Created Submissions
To prevent duplicate Submission records, if Case details are changed, Vault Safety only regenerates a Submission record if one does not already exist for the same Transmission Profile
To regenerate a Submission record to replace one that already exists, mark the Submission record inactive, and then trigger the Evaluate Reporting Obligations action, for example, by moving the Case back to the Approved state.
Manual Creation
While Vault automatically creates Submissions based on configured reporting rules, you can manually create Submissions for ad-hoc reporting, such as amendments or nullifications.
Create a Submission
- On the Case that you want to submit, expand the Transmissions section, and then select Create.
- In the Create Transmission window, select Submission, and then select Continue.
- Complete the fields on the Create Submission page, as required. Submission Fields provides more information.
- Select Save.
Result
Vault creates the Submission and creates a Review Submission task for users in the Distribution Manager role.
Submission Fields
Field | Description |
---|---|
Transmission Profile | Select the Transmission Profile configured for submitting ICSRs to the destination agency. Depending on your Admin's configuration, selecting the Transmission Profile automatically populates the following fields:
|
Origin | Select the organization set up as Vault Customer (vault_customer__v ) for your Vault. |
Destination | Select the destination agency to which the report will be sent. |
Transmission Document Type | Select ICSR document format to generate for the transmission.
For Gateway Transmissions, select an E2B format. For more information on which report formats to generate for different regulatory agencies, see the report formats detailed on Standard Agency ICSR Submissions. |
Additional Transmission Document Type(s) | If required, select additional ICSR document formats to generate for the transmission. |
Sender (User) | If your Admin has configured the Transmission Profile to populate this field with a default Sender User, this field is automatically populated on the Transmission. If this field is left blank on the Transmission Profile, it is populated with the person assigned the Head of Safety sharing role. |
Transmission Reason | The reason for submitting this ICSR to the agency. This field may be automatically populated based on the reporting rule or the Case-level value.
You can select from the following options:
Note: If a value has been entered in the Transmission Reason field of the Case, that value is overridden by selecting a value in this field. |
Reason Text | For nullification and amendments only, enter more information about the submission reason. This field may be automatically populated based on the Case-level value.
Note: If a value has been entered in the Transmission Reason Text field of the Case, that value is overridden by selecting a value in this field. |
Due Date | The Submission due date is automatically generated based on the case attributes and reporting rule for the jurisdiction. |
Local Expedited Criteria | Whether the Case requires expedited reporting, according to agency-specific criteria. For example, the FDA's local expedited criteria for post-market cases is serious and unexpected. Vault automatically sets this field after matching the Case to the appropriate reporting rule. You can manually edit this field to override the Vault-set local expedited value. This field does not appear on layouts by default, but can be added to Transmission layouts by your Admin. |
Downgraded | Marks Cases that match a downgrade scenario. Vault automatically sets this field after matching the Case to the appropriate reporting rule. A downgraded case is a Follow-Up Case that does not fulfill local expedited criteria (Local Expedited Criteria=No), but has a preceding Case version with a Transmission that meets the following conditions:
This field does not appear on layouts by default, but can be added to Transmission layouts by your Admin. |
Organization | Vault automatically populates this field when you create a Transmission from a Case. |
E2B Message ID | Message ID to use in the E2B message header. Vault automatically populates this field with a message ID when the Submission is manually created or the Submit to Gateway action is triggered. |
Destination Case ID | Vault automatically populates this field upon receipt of the final acknowledgment (ACK) when you export E2B Submissions. |
Transmission Date | The date of transmission. Vault automatically populates this field with time and date of submission when the Submit to Gateway action is triggered.
This field is required for EMA submissions. |
FDA Report Type | For manual submissions using the FDA 3500A form, you can optionally use this field to specify the report type. The value in this field populates the appropriate checkbox in box G.7 Type of Report. If you don't specify this field, Vault automatically calculates G.7 Type of Report. For more information, see the description on the applicable FDA MedWatch 3500A format. |
Report Type Override | When reporting to the EMA, you can override the Report Type. This is useful, for example, when a Clinical Trial Case involves adverse events related solely to non-investigational medicinal products available in the EU. Select a Report Type from the picklist. When generating EMA E2B(R3) reports, the C.1.3 Type of Report data element is populated with the corresponding code. This overrides the value in the Report Type field on the Case. Additionally, if Report Type Override is set to Spontaneous, the C.5 Study Identification block is not generated. For more information, see E2B Generation Data Mapping: EMA E2B(R3). |
Auto-Submit | Select Yes to enable automatic Transmissions directly from the Case.
Leave this field blank to require users to trigger the Transmission manually from the Submission or Distribution record. Your Admin may need to configure this field to appear in your Vault. Auto-Submissions provides more information. |
Follow-up Number | Vault automatically populates this field. The Follow-Up Number is based on the number of previously completed Submissions to the same reporting destination for the Case, including previous Case versions. Prior Submissions must be in the ACK Accepted or Completed state to be counted. You can manually override the value, however, this field is hidden by default. Your Admin can add this field to the layout, or you can add the field to the grid view on the Submissions tab. Note the following considerations about the Submission Follow-up Number:
|
Transmission Messages | Contains any acknowledgments being sent in the submission process. The initial "Creation Message" captures the outcome of the rule engine. |
Attachments | Contains a CSV attachment file which displays schema validation errors. |
Registered As | Select the product type classification for generating the ICSR document. Depending on your Admin's configuration, this field may be called Transmission Product Type. For Combination Product reports, the value in this field determines whether Device-type Product Constituents are exported in the E2B file. If this field is left blank or set to Combination Product, the device constituents are exported. Otherwise, only non-device Product Constituents are exported to the E2B file. See Exclude Device Constituents from E2B Exports for more information. |
Safety Report Version | The version of the safety report. This field populates the < This field does not appear on layouts by default, but can be added by your Admin. |
Message Type (HC) | For submissions to Health Canada, you can use this field to select the Message Type (M.1.1) to populate when generating a transmission document in the HC E2B(R2) format. This picklist contains the following standard options:
This field set to the following default values when using standard Health Canada Transmission Profile:
This field does not appear on layouts by default, but can be added by your Admin. |
Patient Content Protection | (Optional) To mask patient data in the generated safety report, select a masking option. Mask Personal Identifiable Information (PII) describes the data masked by each option. This field does not appear on layouts by default, but can be added by your Admin. |
Exceptions to Patient Content Protection | (Optional) To leave certain information unmasked when using Patient Content Protection, select one (1) or more fields to unmask. Exceptions to Patient Content Protection describes the data unmasked by this option. |
Validation Status | The calculated Validation Result for the Submission. The following list describes the Validation Status field values:
Note: You cannot trigger the Submit to Gateway action if the Validation Status is Hard Fail. Vault will not trigger auto-submission if the Validation Status is Fail or Hard Fail. To learn more, see Case and Submission Validation. |
Next Steps to Complete the Transmission
Once you have created the Submission record, you can proceed with handling the Transmission using one of the following methods, depending on the type of Transmission Profile being used: