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Stocks Under $10 with 50-100% upside potential - 14 days FREE!

LORENZ DrugTrack Solution: Take A Closer Look

Do you know the value of your data? drugTrack EVMPD works flawlessly as a stand-alone solution. Yet the software will yield significantly more added value when purchased as part of drugTrack PRO which will allow you to re-use your xEVMPD data for other important regulatory information tasks.

Manage your full regulatory lifecycle The system presents an opportunity for companies to manage all regulatory affairs information with a single system, saving both cost and time in the process. LORENZ drugTrack PRO can use a company's accumulated data to track the entire regulatory lifecycle on both the national and European levels, thus eliminating the time and cost of maintaining two parallel tracking systems.

Identify the impact of changes in your product composition In addition, drugTrack offers cost-saving features such as batch reporting. When a variation such as a change in a supplier address arises, drugTrack can generate a report of all registrations affected by the change, market by market, and generate the variation reports to all of the relevant national authorities.

Plan your regulatory strategy The entire drugTrack system was originally developed together with a pharmaceutical company to satisfy their regulatory tracking needs. It provides a level of security and complexity that the traditional range of spreadsheets, calendar entries and handwritten notes simply cannot. In that scenario, spreadsheet data can be changed accidentally with no control, multiple versions of the same sheet can circulate at the same time, and there is no consistent system for reminders and deadline alerts. drugTrack integrates all of this into a single database system where every step is tracked and remains transparent. Marked entries highlight where changes have been made between versions. And notifications and reminders ensure that no deadline is missed.

The LORENZ drugTrack system will also support the global ISO Identification of Medicinal Products (IDMP) format when it comes into force.

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