CRO 360º

In order to obtain results from an idea of a clinical study project as registration dossier, CE marking or publication we need a great deal knowledge and specialization in clinical research, as well as the involvement of a large number of professionals specialized in their areas.

This requires a multidisciplinary team that works according to standard operating procedures unique to the entire project, from the protocol design to the final report and subsequent publication.

Experior CRO 360º is a comprehensive service in which we cover any aspect related to clinical research in phase I to phase IV trials, post-marketing studies and studies with medical devices. The difference is the flexibility, since we go out of our way to meet the client’s needs. A flexibility that allows us to work together or separately with the client’s employees creating a fully integrated project team.

This is how Experior becomes to be the ideal partner in Spain.

CRO 360º expressed in figures, since 2013

Years of experience

National projects

International projects

Sites managed

Therapeutic
areas

Methodology

We are experts in the design of clinical trials and observational studies.
We go out of our way to meet the client’s needs, we can work with our own procedures or with the sponsor’s procedures.
We have experienced and highly qualified staff in the most popular therapeutic areas: Oncology, hematology, neurology, cardiovascular, etc. as well as in medical devices.
We have a quality management system that meets the highest standards. ISO 9001:2015.

The first step is to have a kick-off meeting with the sponsor to ensure the establishment of the study milestones and the schedule.
We adjust our tasks according to the planning of the project, establishing objectives and deadlines.
We have the ability and experience to work and manage a large number of studies, sites and patients at the same time.
We provide the sponsor and those involved in the studies with real-time reports of the project status, submission procedures, recruitment, monitoring visits, data management, and safety data thanks to our automated reports.

Phases

Planning with the Sponsor.

Establishing the tasks, deadlines and results to obtain.
Study design.

Drafting of documents and creation of tools (eCRF, eTMF, logistics, etc.) required to obtain expected results in the shortest possible time and with the highest quality.
Study submission procedures.

Obtaining the regulatory authorizations, including the contracts required to start the study in accordance with the current regulations.
Operational development of the study protocol.

Monitoring, pharmacovigilance and data management in real time. Always based on risk.
Exploitation and publication of results.

Performing the planned statistical analyses required for drafting the final reports and the necessary publications.