What's New in Software Releases

LORENZ drugTrack now supports the full data entry, tracking, and submission workflow for Medical Device Applications, built around the business objects and structure you already work with. The LORENZ Dashboard serves as your central setup point for Medical Device Registration tracking, with the Medical Device Application as the main object to manage your registrations. Whether you're preparing submissions for the EUDAMED gateway or simply getting your data in order, the system is ready to support you end to end.

LORENZ drugTrack supports the EUDAMED data model, managing your medical device data in a fully compliant way, including the UDI and device registration module. With medical device registration in EUDAMED rolling out from Q2 2026, now is the right time to get your data structured and your processes in place. drugTrack reduces manual data entry, improves data quality, and maintains audit-ready logs, so when the deadline arrives, you're not scrambling, you're already there.

Compare View now covers the full depth of a record down to the last detail, with each change highlighted by color and optionally by icons via the new “emphasize comparison” toggle. Full data comparison between two records has never been this straightforward.

When LORENZ drugTrack introduced PMS Enrichment last year, it became one of the first solutions to support the EMA's Product Management System directly, letting you meet PMS requirements without re-entering product data in the PMS UI. Now, that capability gets even more practical: Administrators can configure multiple PMS Client IDs and map each one to its corresponding OMS ORG ID. If your organisation operates across multiple entities or markets, the setup now reflects how you actually work.

The new PMS enrichment feature enables the data enrichment process for the European Medicines Agency's Product Management System (PMS). drugTrack is among the first solutions to support this, allowing you to meet EMA's new PMS requirements directly within the system, without re-entering product information in the PMS interface.

The new batch apply function for Proposed Marketing Authorisations lets you apply multiple internally approved Regulatory Activities at once. This saves time and reduces repetitive manual work when managing several proposed MAs in parallel.

The volume operations in drugTrack now include the options Volume Activate and Volume Deactivate, allowing you to update several records in a single step. This makes it faster and easier to manage large data sets and keep your records up to date with minimal effort.

The new comment feature lets you easily communicate and align with colleagues without leaving drugTrack. Mention users to notify them instantly, reference specific fields, and add hyperlinks to provide clear, actionable context. By keeping conversations close to the data, this feature reduces back-and-forth and even improves cross-functional workflows.

You can now create and edit multiple Proposed Marketing Authorisations and their related Regulatory Activities in one step. The "Create proposal" option allows you to prepare changes without directly editing records. This makes bulk editing and bulk creation of Marketing Authorisations faster, easier, and more controlled.

The latest release brings a refreshed look to the LORENZ RIM web interface with improved accessibility and customization. The modern theme is now available in light and dark Modes, with updated colors that meet Web Content Accessibility Guideline standards. New options let users adjust contrast, font size, and spacing to suit their visual and working needs. An experimental theme named “Innova” also adds more flexibility with customizable color and shape settings, offering a more tailored experience for you.