CROLLL
  • Crolll - Firmensitz

eCRF-DESIGN AND MANAGEMENT

We develop user-friendly, intuitive input forms that maximize data quality and minimize sources of error.

Regulatory affairs

We handle the preparation and submission of your clinical trials via CTIS or DMIDS.

Project management

We handle the planning and management of clinical trials, non-interventional studies, and other research projects.

Monitoring

Our experienced monitoring team covers all areas of monitoring throughout Germany.

Medical / scientific writing

With our team of experienced scientists, we produce accurate and expert texts and conduct literature reviews, for example.

WELCOME TO CROLLL

Our first priority is the legally compliant, swift and seamless implementation of partial or complete solutions for trials involving pharmaceuticals and/or medical devices, in order to meet the ambitious timelines of our clients.
Meet our experienced and dedicated team.

  • Individual

    individual solutions, targeted to your projects

  • Flexible

    flexible management of a clinical study / support in the scientific area – Full Service or sections

  • Obliged

    personal obligation of our team towards your project

  • Experienced

    Highly-qualified, experienced team

  • Quick

    Quick processing and adjustment to new conditions

Our focus is on providing a service tailored to your specific needs to ensure the efficient execution of your project. The excellence of our service is rooted in our personal commitment and dedication to your project. Since our founding in 1998, we have successfully completed nearly 1,000 projects.