In its history spanning more than three decades, CRS has developed particular expertise in the recruitment of challenging populations in terms of sample size (> 200 subjects) and specification (patients, postmenopausal women, senior citizens, etc.) as well as the implementation of challenging trial designs regarding follow-up activities (e.g. long-term examination up to two years), long hospitalisation periods up to 53 days and clinical assessments (e.g. cardiovascular, respiratory, dermatology and women's and men's health).
Together with its strict Phase I standardised environment and internal QA and QC procedures, CRS is able to handle multi-centre settings within CRS under most possible standardised conditions.
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