Why DLTA?

Integrate • Automate • Optimize

Why Struggle with a Drug Development Life Cycle from the Stone Age?

Let’s be honest, navigating Drug Development projects isn’t for the faint of heart. It’s a stringent and complex enterprise. To make matters worse, most teams still rely on Excel spreadsheets to store critical data, time wasting meetings to assign work, and long email chains to update statuses. To top it off, there’s chronic unpredictability of project handoffs and budget tracking.

Take Control. DLTA removes inefficiency and complexity from the clinical trial project and all other processes that work in conjunction with the clinical program and regulatory submission process. The result is an intuitive and adaptive central platform that helps you get your products to market faster and more easily.

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Organizational Benefits

benefits

  • Minimize budget overruns by providing 100% visibility and accountability into every task related to all active products in the pipeline, their projects, tasks, approvals, documents, priorities, and progress in real time.
  • Reduce FDA compliance challenges caused by missed deadlines or incomplete information by consolidating 130+ processes into a single, secure, scalable, and integrate-able platform.
  • Reach market approval months faster by optimizing business processes, enforcing regulatory compliance, and automatically compiling the documentation for your eCTDs, EDC, and eTMFs.

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Take Control with DLTA

Instead of the disconnected teams and dropped responsibilities, DLTA delivers a pharmaceutical development process that’s simple, manageable and efficient. Want to know more? Contact us.

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