Healthy Volunteer Studies
CRS conducts early-phase clinical studies in healthy volunteers as part of Phase I clinical development programs. Studies are designed and conducted in accordance with applicable ethical standards and regulatory requirements within the European Union.

Volunteer recruitment & management
An established volunteer pool and structured screening processes support efficient participant identification and study enrollment. All volunteers are evaluated according to protocol-specific inclusion and exclusion criteria prior to study participation.Study participationHealthy volunteer participation is coordinated and supervised by qualified medical staff, with study activities conducted in a controlled inpatient environment appropriate for early-phase clinical research.

Study participation
‍Healthy volunteer participation is coordinated and supervised by qualified medical staff, with study activities conducted in a controlled inpatient environment appropriate for early-phase clinical research.
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• Medical supervision by experienced clinical staff
• Ethics committee approval for all studies
• Clear information and informed consent
• Financial compensation for participation