Skip to end of metadata
Go to start of metadata

You are viewing an old version of this page. View the current version.

Compare with Current View Page History

« Previous Version 10 Current »

📲 Share or Open on Web

TrialKit can support any risk-based monitoring (RBM) models that are created outside the system in analytical or biostatistics reporting. This takes Field Source Verification to a more site/subject-specific level, rather than applying the same rules throughout an entire study. In other words, a study manager may want Monitors to verify specific data points that need review, but those requirements may vary by site or even by subject. 

This article covers how to configure which fields require source-level verification under a risk-based monitoring model.

Rules for what needs to be monitored are easily defined directly from the CRFs in the study. This can be done on any CRF at any site depending on what rules are being defined. The options per rule are as follows:

  • Starting date

  • Distribution: Single participant, single site, all sites

  • Single-visit or all visits where the form exists

To define a new rule, open an applicable subject record that will need to be monitored. Tap the workflow settings icon indicated below.

The ability to see this icon depends on access to configure risk-based monitoring from the study role security settings.


As shown in the image below:

  1. Tap the lock icons next to any of the fields on the form that need to be Monitored. 

Green = enabled (Monitor will review). 

Red = disabled (Monitor will not review)

2. Once the desired fields are set, tap the icon in the upper right corner. This is where the rule will be defined and saved. 


To define and save the new rule, indicate a starting date and which forms the rule will apply to, and then define which subject and record(s) the rule is for.

The starting date for the rule is compared to the visit/transaction date on the form, not the current date when Monitoring takes place.

The following are the rules that can be applied:

  • All participants in the study

  • All participants at the current site only

  • Just the participant currently open

  • All visits where the current form is collected

  • Only the record that is currently open

To edit an existing rule, tap it in the Existing configurations table and change any of the parameters listed above. Then tap Save.

In the configuration above, monitoring will be required on the first three fields of the form for records with visit dates starting on March 24, 2018, for all subjects at one site for one visit.

Related articles

  • No labels