LORENZ drugTrack logo
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Software Status:Active
Web, Windows
LORENZ Life Sciences Group Birkenweg 10 64297 Darmstadt Germany
Email · Phone
All Countries

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. It offers features like server capabilities, comprehensive reporting, and user management so that users can effectively manage regulatory submissions and track compliance. With over 2000 paid installations in 48 countries, including 19 health authorities, LORENZ drugTrack is a proven solution in the market. The software supports various regulatory activities, ensuring that users can simplify their processes while maintaining compliance with industry standards. Key capabilities: server integration comprehensive reporting user management regulatory submission tracking compliance monitoring Best for: pharmaceutical companies and regulatory agencies that need to manage and track regulatory information efficiently.

LORENZ drugTrack Details

Vendor
LORENZ Life Sciences Group
Year Launched
1989
Location
LORENZ Life Sciences Group Birkenweg 10 64297 Darmstadt Germany
Deployment
cloud, on premise, windows, web browser
Training Options
documentation, live online, in person, demo, account manager, community
Countries Served
All Countries
Languages
English, German, French, Spanish, Italian, Japanese, Chinese
Users
Regulatory affairs specialists, Pharmaceutical companies, Health authorities, Academic researchers
Industries Served
Pharmaceutical, Healthcare, Life Sciences
Tags
Product Lifecycle Management, Regulatory Compliance, Pharmaceutical Industry, Submission Management, Electronic Document Management

LORENZ drugTrack's In-App Market Place

Does LORENZ drugTrack have an in-app market place?

Yes

How many Mini-Apps in the marketplace?

12

Mini Apps

1. Drug Information Management System (DIMS): This add-on allows users to efficiently manage and track drug information throughout the product lifecycle

ensuring compliance with regulatory requirements.

2. Labeling Software: This tool enables users to easily design

manage

and track labeling for pharmaceutical products

streamlining the labeling process and ensuring compliance with industry standards.

3. Electronic Submission Management System (ESMS): This add-on simplifies the process of preparing and submitting electronic regulatory submissions

helping users navigate complex regulatory requirements and ensure compliance.

4. eCTD Viewer: This tool enables users to easily view and navigate electronic Common Technical Document (eCTD) submissions

making it easier to review and approve regulatory documents.

5. Regulatory Intelligence Database: This add-on provides users with access to a comprehensive database of regulatory requirements and guidelines

helping them stay informed and compliant with changing regulations.

Pricing Options

Free trial
Free version
Request a quote
Promo Offer

Accepted Payment Currencies

USD ($), EUR (€), GBP (£), JPY (¥), AUD ($), CAD ($), CHF (₣), CNY (¥), HKD ($), INR (₹), SGD ($).

Pros & Cons

  • 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.
  • 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.

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