In order for a pharmacy or hospital to dispense medicines or a pharmaceutical wholesaler to distribute prescription medicines in Denmark, they must be connected to the Danish Medicine Verification System (DMVS). Pharmacies, hospital pharmacies and wholesalers must have a contract with the Danish Medicine Verification Organisation (DMVO) before connecting to the medicine verification system via their own existing IT systems.

If your customer’s system is connected to the medication verification system for the first time, you as the user’s IT supplier must sign an NDA (Non-Disclosure Agreement) with DMVO and perform certification before the integration can be implemented in the production environment.  You must also ensure that your customer has requested access to DMVS before the integration is completed in the production environment. You can contact the DMVO-secretariat (info@dmvo.dk) if necessary.

To integrate the verification system in your production environment, you need to do the following:

1. Contact the DMVO-secretariat for information about the relevant registrations and signing of the NDA (Non-Disclosure Agreement).
2. Register for the SSR Developer Portal to review the technical documents (more info below).
3. Perform tests in the Integrated Test Environment (ITE).
4. Perform certification tests in the DMVS Integrated Quality Environment (IQE environment). The testing process for the SSR certification and the required prerequisites can be found in the SSR Developer Portal: link to the portal.
5. After the tests, DMVO provides a final approval (certification) to connect the user’s IT system with the Danish Medication Verification System in the production environment.

You can register on the portal (Solidsoft Reply ITE Developer Portal) by writing to the DMVO-secretariat on info@dmvo.dk.  All representatives of the IT suppliers who have signed an NDA agreement with DMVO and who need information from the portal can register with the Developer Portal.

The Developer Portal gives you access to things like:

1. Overview of the European Medicines Verification System (EMVS) and Solidsoft Reply’s national drug verification system.
2. Information about the Integrated Test Environment (ITE), including the Baseline Testing Guidelines.
3. Guidance on how to implement, qualify and implement the interface to Solidsoft Reply’s national drug verification system.
4. API documentation, including the ability to send API requests to the ITE-environment directly from your browser.
5. The system’s alarm and return codes with descriptions in different language versions and all endpoints also for the different environments in the Danish national drug verification system.
6. Content and latest changes in Medication Verification System version updates and API versions.
7. Contact information for support.