LORENZ drugTrack logo

LORENZ drugTrack

by LORENZ Life Sciences Group · Since 1989
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Active1+ countriesCloudOn-premise
Quick facts
VendorLORENZ Life Sciences Group
Year launched1989
StatusActive
LocationLORENZ Archiv-Systeme GmbH Eschborner Landstrasse 75 60489 Frankfurt/Main Germany
Countries served1+
Languages7
Integrations5+
Free tierNO
Free trialNO
Contact salesYES
Last reviewed: May 2026

About LORENZ drugTrack

LORENZ drugTrack is a regulatory information management software from LORENZ Life Sciences Group designed for the pharmaceutical industry, health authorities, and academia.

LORENZ drugTrack is a regulatory information management (RIM) and product lifecycle management software developed by LORENZ Life Sciences Group, specifically designed for the pharmaceutical industry, health authorities, and academia. The platform serves as a centralized database for managing medicinal products, medical devices, and drug master files throughout their entire lifecycle. Key capabilities include robust compliance management with audit trails, deadline triggers, and four-eyes principle workflows, alongside advanced querying and reporting tools that allow users to visualize data via customizable dashboards. LORENZ drugTrack supports xEVMPD and IDMP compliance, enabling users to generate report messages for the EMA. The system is highly flexible, offering deployment options for both local and cloud environments, and is scalable from single-user setups to large enterprise implementations. LORENZ provides comprehensive support services, including installation, validation, migration, and configuration, alongside various training options such as webinars and on-site sessions. The software is designed to integrate with other LORENZ solutions and third-party systems to facilitate a flexible regulatory information management ecosystem.

Pros & Cons

Pros
  • The system provides a centralized database for managing complex pharmaceutical product information and lifecycle activities.
  • It supports critical regulatory compliance standards including xEVMPD and IDMP data models.
  • The platform offers flexible deployment options including both local and cloud-based installations.
  • Users benefit from built-in quality control features like audit trails and four-eyes principle workflows.
  • The software is scalable to accommodate needs ranging from single users to large enterprise organizations.
Cons
  • Pricing information is not publicly available and requires direct contact with the vendor.
  • The system requires specialized knowledge of regulatory affairs, which may present a learning curve for new users.

Features

Key features

Product Information Database

Effortlessly create, update and maintain medicinal product, medical device, development product and drug master file information.

Compliance Management

Ensure quality control with four-eyes principle, audit trail, deadline triggers, reminders and e-mail notifications.

Product Lifecycle Management

Track the entire pharmaceutical product life cycle using regulatory activities and change control management.

Querying and Reporting

Illustrate your data with dashboard graphics, create your own dashboard and export information using different formats.

xEVMPD and IDMP Compliance

Create and update EudraVigilance medicinal product report messages to the EMA and prepare data in compliance with the IDMP data model.

Additional features

Electronic data capture,
Document management,
Regulatory tracking and reporting,
Audit trail,
Workflow automation,
Collaboration tools,
Integration with other systems.

Pricing

Free trial
Free version
Request a quote
Promo Offer

Countries & Languages

1
Countries served
7
Interface languages
11
Billing currencies

Available in

ALL

Interface languages

EnglishGermanFrenchSpanishItalianJapaneseChinese

Billing currencies

🇺🇸USD🇪🇺EUR🇬🇧GBP🇯🇵JPY🇦🇺AUD🇨🇦CAD🇨🇭CHF🇨🇳CNY🇭🇰HKD🇮🇳INR🇸🇬SGD

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