Solution & Services

Explore Our Solutions and Services

From regulatory services over monitoring to project management, our experienced teams use interdependent relationships to achieve results that go beyond expectations. Explore our integrated solutions, which are designed to streamline business procedures, shorten timeframes, and drive success in all clinical trial endeavors. 

Our Data Management team ensures data integrity from setup to database lock. We provide tailored plans and rigorous quality control to deliver high-quality, compliant datasets for your clinical trials.

Our local teams offer a deep understanding of the regional clinical dynamics, working alongside you to devise an optimal strategy for your study and identifying ideal trial sites through detailed feasibility studies.

We are ready anytime to support you during your peak times with Project Management, Monitoring, Regulatory, and other services. 

Our medical writers, drawing on broad industry and academic knowledge, produce timely, cost-effective clinical and regulatory documents, transforming complex data into an accurate, evidence-based account of your drug’s clinical profile. 

Our teams build strong relationships with individual study sites, and our Clinical Research Associates provide ongoing support from regulatory document collection to data cleaning, driving site success in enrolment goals and high-quality data provision. 

Our Regulatory Affairs Unit, backed by over 25 years of experience, offers operational and strategic consulting services, guiding a product from development through clinical trials to market authorization. 

Our study team collaborates with selected sites to collect essential documents, finalize clinical study agreements, and manage submissions and document preparation in parallel, ensuring maximum site initiation at the study’s outset. 

Harnessing interdependent relationships within an integrated Project Team, our Project Managers oversee project activities, timelines, deliverables, and budget while providing regular study progress updates. 

Need Consultation?

You are facing a challenge in preparation for your clinical trial? We are here to help. Our team is ready to offer tailored guidance. Reach out and let’s get the conversation started. We are committed to finding the right solutions for you.

Your Solutions Contact

Director Business Development

Ralf Freese

  • 23+ years of CRO experience
  • Extensive experience in the conduct of trials as Principal Investigator (PI)
  • Responsibility as Medical Director in over 130 Phase I–III studies