CRS is a full service CRO and offers planning, conduct, evaluation and reporting, in all areas of human pharmacology clinical testing. Specific experience within the respective units is planned to be kept, further developed and expanded to the whole group, where feasible. These are renal and hepatic insufficiency trials in Kiel, QTc trials in Mönchengladbach, skin safety, pain models and respiratory testing in Mannheim.

Human pharmacology services:

·      First in man (FIM),

·      Safety and tolerability

·      Infusion studies, inhalation, s.c., i.m. injections

·      Bioavailability and Bioequivalence

·      Food and Drug interaction / Drug and Drug interaction

·      Pharmacokinetics

·      Dose finding

·      Pharmacodynamic Modelling / Proof of Concept

·      Special patient investigations COPD trials