Our Services

CLIOSS holds extensive experience for the planning and conduction of clinical trials in leading oncology sites in EU and US, a tradition of competences and capabilities in clinical pharmacology and oncology clinical development of
cytotoxics, hormones and targeted therapies, and a successful track record in orphan drug designation.

CLIOSS services are flexible and range from comprehensive drug development management (internal resources) to
assistance with specific stages of the study's implementation or consultancy.

Clinical Program Strategies

CLIOSS is committed to the strategic clinical development, and execution of, clinical trials. With a long-term expertise in designing, conduction and data analysis, we provide an effective support in obtaining conclusive study results, meeting regulatory submission requirements.

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