Configure Watchlists to flag and monitor Adverse Events of Special Interest (AESI) under a product or study.
About Watchlists
Set up a Watchlist to monitor Adverse Events of Special Interest (AESI) and other Important Medical Events (IMEs). You can configure Watchlists to always expedite Cases, regardless of the Case expectedness or causality.
Watchlists can be created for marketed products, combination products, or studies. They can also be created without being based on a product or study. Cases with an adverse event that matches a Watchlist MedDRA term are tagged with the appropriate Watchlist Tag during Case processing in the Watchlist Tags field.
Designated Medical Events (DME) Watchlist
The official DME Watchlist is available by default in all Vault Safety Vaults. By default, the DME watchlist monitors only Cases with a product or study registered in a country under the jurisdiction of the EMA.
When a Case Adverse Event MedDRA term matches to an entry in the DME Watchlist, Vault Safety tags the Case as a DME and expedites the reporting due date. Any MedDRA term is considered a match if it is listed on or falls under the hierarchy of the term on the Watchlist.
Prerequisites
- You must be an Admin to manage Watchlists.
- Ensure that your Vault has the Adverse Event Watchlists feature enabled.
- To support hierarchical browsing of MedDRA Terms, we recommend making some criteria VQL updates in your Vault. Contact your Admin to enable MedDRA UI Enhancements for Non-Case Coding
- To use MedDRA Queries to add a large group of adverse events from a combination of SMQs, CMQs, and MedDRA Terms at once, your Admin must enable MedDRA Query Building Blocks.
To ensure access to Datasheets, the MedDRA Criteria object must be configured so the Organization field is mandatory.
Make the Organization Field Mandatory
- Go to Admin > Configuration > Objects > MedDRA Criteria > Object Types.
- Go to the Watchlist Field Criteria object type, and then select the Organization field.
- In the Organization field, ensure User must always enter a value (required) is selected. Do not modify the Criteria VQL.
- If watchlists were already added to your Vault before enabling this setting, go to each watchlist and manually specify the Organization field in the System section.
Note: If you don’t see the Watchlist Criteria object type, add this object type under the MedDRA Criteria object. Contact your Veeva Services representative for assistance.
Result
The system will automatically populate the Organization field for all new MedDRA Criteria records, using the default Criteria VQL.
Set Up a Watchlist
To set up a new Watchlist, create the Watchlist, and then add the Case field updates. When you save the Watchlist, the MedDRA Terms and MedDRA Queries sections appear. By adding MedDRA Criteria and MedDRA Query records in these sections, you can list adverse events to be watched.
Create a Watchlist
- Go to Business Admin > Objects > Watchlists.
- Select Create.
- On the Create Watchlist page, complete the following fields:
- Organization: Select the organization that monitors the watchlist.
- Name: Enter a name for the watchlist.
- Watchlist Tag: Select a Watchlist Tag with which to label Cases that match this watchlist.
- Study: (Optional) To monitor cases associated with a study, select the Study.
If you select a Study with Unspecified Products, Watchlist Tags are applied to Case Products with a Drug Role of Suspect or Interacting on Cases for that Study. - Study Product: (Optional) For study watchlists, to watch Cases associated with a specific study product, select the Study Product.
To enable this field, you must first select the Study. - Product: (Optional) To monitor Cases associated with a marketed product, select the Product. If you select a Combination Product, the system automatically monitors Cases containing its Product Constituents. A Case Product must link to this product with a Drug Role of Suspect or Interacting to trigger a watchlist.
- MedDRA Version: Select the MedDRA version to use when adding MedDRA terms to the watchlist.
- Watchlist Exclusions: (Optional) Select Clinical trial studies from the picklist to exclude Cases with the Study Type field set to Clinical Trial
(clinical_trial__v)
from the Watchlist.
- Select Save.
Note: Specifying a Product or Study is optional. If you choose to specify one of these fields, note that you cannot complete the other. Otherwise, the Watchlist can not run.
Note: Exclusions may be applied only when Watchlists do not specify a Study or Product.
Add Updates to Case Fields
Configure your watchlist to automatically set the Expedited and Seriousness values for Cases with matching adverse events.
- On the Watchlist page to which you want to edit, expand Updates to Case Fields.
- On the Updates to Case Fields section, complete the following fields:
- Expedited: To expedite the reporting timeline for Cases that match this watchlist, select Yes.
If you enable this option, Cases will be expedited regardless of expectedness or causality. - Default Seriousness: Select the Seriousness criteria.
- Expedited: To expedite the reporting timeline for Cases that match this watchlist, select Yes.
- Select Save.
Result
Any Cases matching the watchlist criteria will be automatically assigned the set Expedited and Seriousness value. For example, an Inbox Item with a matching adverse event will be assigned these values by the watchlist upon Case promotion.
Note: If the Inbox Item being promoted already has a specified Seriousness field, the watchlist will not update it upon Case promotion.
Add MedDRA Terms
Configure individual adverse event terms for the watchlist.
Adverse events can be added to Watchlists at any level of the MedDRA hierarchy. When Case Processors code adverse events on Cases, any MedDRA LLT is considered a match if it is listed on or falls under the hierarchy of the term on the Watchlist. For example, if the Watchlist includes the HLGT “Allergic conditions” as an adverse event, then the Case-level LLT “Drug-cross-reactivity” would fall under the Watchlist-coded HLGT term and a Watchlist tag would be added to the Case Adverse Event.
- Go to the Watchlist record.
- Under MedDRA Terms, select Create.
- In the Create Watchlist Criteria window, complete the fields.
- Select Save.
- Repeat for any other applicable MedDRA terms.
Result
Your Watchlist is now configured to watch the specified adverse events. Inbox Items with matching adverse events will be updated with the criteria set in the Watchlist (Watchlist Tag, Seriousness, Expedited) upon being promoted to a Case.
Watchlist Criteria Fields
Add Watchlist MedDRA Queries (MedDRA Query Building Blocks)
MedDRA Query Building Blocks offer a way to combine existing Standard MedDRA Queries (SMQs), hierarchical MedDRA terms, and Custom MedDRA Queries (CMQs) in a MedDRA Query record. The MedDRA Query with the building blocks can then be applied to multiple Datasheets and Watchlists, and all of the MedDRA terms within the building blocks are added to those records. Vault considers only SMQ terms with the same MedDRA Version value of the Watchlist or Datasheet. Admins control when to push MedDRA Query record changes to all Datasheets and Watchlists using it.
Add each MedDRA Query record under the Watchlist:
- Navigate to Business Admin > Objects > Watchlists.
- In the MedDRA Queries section, select Create.
- Select the appropriate MedDRA Query.
- Select the Scope. Select
Narrow
orBroad
to pull in values with the corresponding scope applied on the SMQ or CMQ term. Leave this field blank to pull in all values. - Select Save.
- In the All Actions menu, select Update from MedDRA Queries.
Result
The MedDRA Terms section includes all MedDRA LLTs that fall under the MedDRA Query record.
Add Watchlist Tags
By default, Vault Safety includes two Watchlist Tags: DME and AESI.
To add custom Watchlist Tags, configure the Watchlist Tags picklist to add new options. Managing Picklists provides more information about configuring picklists.
Watchlist Questionnaires
After configuring a Watchlist, you can configure Watchlist questionnaires to allow Case processors to quickly send an automated email to case reporters for follow-up information. You can set up the questionnaire for the entire Watchlist or for specific MedDRA Terms within a Watchlist. Set Up Scheduled Follow-Up Questionnaire Emails provides more information.