Experior has an extensive experience and a highly qualified staff that allows covering any area related to clinical research in Phase I to Phase IV studies. Experior offers a flexible, customized service that meets project and client needs. We are able to carry out an entire project, from the protocol design, study coordination, data management, and statistical analysis to its final report. We can even adapt ourselves to the level of assistance required by our client. This flexibility allows working together with the client’s staff, or separately, creating a completely integrated project team in accordance with the corporate culture of the client.
- Protocol design
- Feasibility of the study
- Project management
- Management of study material
- Management of study medication
- Management of biological samples
- Investigator and site recruitment
- Regulatory proceedings
- Investigator contract and payment negotiations
- Organization of investigator meetings
- Site initiation
- Training of the site staff
- Monitoring
- Site closure