CROLLL - Services
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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.

Our Services

We offer a comprehensive range of services covering all administrative and regulatory aspects of clinical trials involving drugs and medical devices, as well as non-interventional studies and other research projects. Depending on your specific needs, we can manage a clinical trial from start to finish —from planning, execution, and monitoring to data analysis— or handle specific tasks.

  • Project management
  • Regulatory affairs
  • eCRF-design and management
  • Medical / Scientific Writing
  • Monitoring
  • Data management / Biometry
  • Indication expertise / Experience

  • 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

Services