Services

Preparation of documents for implementing, conducting and reporting clinical research.

Development and implementation of processes for collecting, validating and storing clinical data.

Trasnsformation, standardization (CDISC) and reporting of clinical study data.

Definition and implementation of statistical analysis of clinical data, as well asinterpretation of results.

Identify and qualify the best sites for your study. Handle all regulatory submissions/interactions.

Training, controlling and monitoring of your study sites’ activities to assure full compliance with your study protocol.