A Data Protection Impact Assessment (DPIA) is a process that helps organisations identify, assess and manage risks related to the processing of personal data. The purpose is to ensure that the processing is necessary and proportionate to its objectives while protecting individuals' rights and freedoms.
A DPIA is required when a type of processing is likely to result in a high risk to the rights and freedoms of individuals (GDPR Article 35). This is particularly relevant when using new technology or when the nature, scope, purpose and context of the processing suggest a significant impact. A DPIA helps ensure compliance with data protection regulations and demonstrates that the organisation has taken the necessary measures to meet legal requirements. Use a Pre-DPIA to find out whether a DPIA is needed.
To conduct a DPIA, organisations should follow these steps:
It is essential to document the entire process and involve relevant stakeholders, including the Data Protection Officer (DPO) and senior management, to ensure a thorough and effective assessment.
For detailed guidance and checklists, visit the Norwegian Data Protection Authority’s website: datatilsynet.no.
Go to Privacy > DPIA in the left menu. The page lists all registered DPIAs. You can start a new DPIA in several ways:
Each row has a button to Start, Continue or View the DPIA, and View Pre-DPIA when the DPIA was created from one. To create and edit DPIAs you need a role such as User Privacy or administrator.

The DPIA process has five steps: Registration, Privacy Principles, Privacy Risk Assessment, Treatments & cost-benefit and Sign and approve. You can move between the steps in the stepper at the top of the page.
In step 1 you record information about the impact assessment:
This step documents how the processing complies with the privacy principles. It covers:
When the DPIA assesses a processing activity, Diri fills in several step 2 fields from what is already registered on that activity, so you do not have to write the same information twice. The notice Some fields have been suggested from your linked DPA registration is shown at the top of the step.
Fields that can be suggested include the purpose, the types of personal data, whether special categories are processed, the origin of the data, the legal basis, the categories of data subjects, how individuals are informed, and transfers outside the EEA. How much is suggested depends on how much is filled in on the processing activity; a lean registration for a data processor gives fewer suggestions.
The suggestions are a starting point, not your assessment. Read each one, adjust it to what is true for this DPIA, and fill in the questions that call for your own judgement – such as necessity, data minimisation and the impact on individuals – before you click Next. Once step 2 has been saved, your saved answers are what the DPIA shows.
In this step you carry out the risk assessment. Note that it is privacy risks – risks to the individuals whose data is processed – that should be assessed.
Start by identifying undesirable events, their causes and the consequences that may follow. Use Add guided risk to be guided through a risk, Add from template to add events, causes, consequences and treatments from a template, or Import rows to import them.

Then propose risk-reducing measures (treatments), both preventive (proactive) and impact-reducing (reactive).

Switch between Table view and Bowtie view to see how events, causes, consequences and treatments are connected. When you are done, click Finish risk assessment, or choose Save and close to finish later. See Risk assessment for more about working with risks and bowties.

The risks you register appear in Privacy > Privacy Risk Registry, together with the privacy risks from your other DPIAs. See Risk registry and Risk acceptance.
The treatments you documented in the risk assessment are collected in a treatment plan.

For each treatment you can record who is responsible, the cost of implementation, the deadline and the expected risk reduction, so you can weigh cost against benefit. Click Finish treatment plan when the plan is complete. The treatments are followed up together with your other treatments, see Treatments.

In the last step, the treatment plan and the DPIA are approved and signed by the person responsible in the organisation. You can sign yourself if you have the right, or send the DPIA for signing to someone else. For a DPIA, signing includes:
Signing sets the review period for the DPIA. If the risk figures later change so that the conclusion on prior consultation would be different, the signed DPIA says so, and you should review the risks and sign again. Read more in Signing and review.

Each DPIA has a dashboard that gives an overview of the assessment:
DPIA reviews also appear in the Annual wheel, so you can see when each DPIA is due for review.