For
the conduct of non-interventional studies for different target groups we offer:
Planning and design of the observation plan
Design of CRFs for data documentation
Administrative/logistical preparation and handling
Cooperation with the sales representatives of the sponsor
Training of the sales representatives
Organisation of meetings
Training and support of the health practitioners/hospitals
Quality assurance
Data management
Biometrical evaluation of data
Writing of a report
Presentaion of data
Composing of a script for publication
The Quality in planning as well as of the conduct of a NIS is the determining factor for the significance of the results. Only the highest quality standards guarantee optimal results.
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