Since several years High Research supports the investigators and institutions in the realization and management of no-profit interventional and observational clinical trials. The cooperation with universities, hospitals, scientific societies and patient associations allowed us to deeply understand and deal with the dynamics and problems belonging to this kind of studies.
We are able to provide a full range of services for the development of a no-profit study, from protocol writing to the achievement of the ethic-regulatory authorizations, from monitoring to simple and low-budget eCRF production, from statistical analysis to the final report and scientific articles for eventual publications.
We firmly believe that the quality of independent clinical research should have the same standards of excellence as the profit research. The unmet need of the Investigator who has an idea of trial is to have an organization which develops her/his idea in a concrete and precise way.
Our objective is to provide a product tailored to the needs and details of each own project.
Our services to support the Investigator:
- protocol writing
- EudraCT and OsSC (Osservatorio per la Sperimentazione Clinica dei Medicinali) registration
- ethics and regulatory
- monitoring and project management
- statistical analysis and data management