ethica CRO provides a complete range of clinical study management and biometrics services for clinical phases I-III. Services can be contracted either as a comprehensive package to manage your entire study, or on a selective basis when additional resources and services are required.
ethica CRO has extensive experience designing and conducting therapeutic intervention studies using various designs (e.g., parallel, crossover, factorial, adaptive, etc.). Our expertise ensures that the design of the study and its resourcing are optimized to meet the Sponsor's clinical objectives and budget.
For Phase I studies, we partner with clinical pharmacology units that have been pre-qualified based on our accredited SOPs.