Our Experience & Expertise

Having worked on a wide range clinical studies across various therapeutic areas, STATProg provides experienced and dedicated partners with expertise in Phase I to IV studies, regulatory submission support (including ISS and ISE), and CDISC compliance.

Phase I – IV

Looking for top quality service? You’ve found it.

Your clinical trial is the result of many years of development and major investments of your company.

To be sure to get the best out of it you need experienced partners because your clinical study should not be a business trial!

Our team consists of experts in the preparation, set-up, managing and performance of international clinical trials I – IV. We are the partners that you can rely on and help establish milestones and budgets. Your study is our mission and becomes the commitment of our engaged staff.

We adapt responsively to change in your clinical trial to minimize risk and drive quality outcomes.

Clinical research is complicated and it’s easy to get off track due to inexperienced project leaders, inflexible workflows, or the failure to identify risks before they become issues.

We derive expert insights from evidence-based processes and strategic services to be the driving force behind quality outcomes including, optimized data, patient safety, reduced time-to-market and operational savings.

HOW WE DO IT
We are a quality-certified organization supporting the drug development efforts of pharmaceutical and biotech companies. Built on decades of clinical leadership and expertise, we are dedicated to a collaborative approach that accelerates the development of safe and effective treatments.

It’s time to launch your clinical trial project into a whole new level!