What we do

Study protocol including synopsis, protocol, ethical and regulatory aspects, statistical planning

Study coordination including administration, internal project management and coordination

Questionnaire, explanation data collection, data transportation, Database-set-up

Data management, IT (Validation, Data Entry, Coding, Query Management)

CRF design, Materials (questionnaire, postage envelope), Analysis of data

Contract Coordination, creation, signing

Collection of site-specific documents

Patient information and informed consent in German

Biometrical evaluation and study report

Ethics committee Application and fees

Publication, preparation of manuscripts

End of study Report of the end of the study to ethics