Clinical Investigations and project management
We have extensive experience within clinical Investigations and evaluation and will manage your submissions to the authorities and ethics committees and follow the ongoing clinical study.

Clinical Literature Evaluation
Is an important part of the strategy and protocol design. The review is written according to existing guidelines and within multiple clinical applications.

Clinical Trial Documentation
Investigators brochure, final report and publications are designed and written according to international standards and guidelines.

Bio-Statistics
Experienced partners within the bio-statistical field will set up the needed statistical scenarios for your project.

Monitoring
Clinical study monitoring is performed by well educated and experienced staff (Senior Clinical Research Associates) according to GCP guidelines.