What do they think of us?
We promote research by offering comprehensive support in the management and implementation of clinical studies.
We provide advice, solutions and structures that accompany the investigator throughout the clinical study process, from design to execution, guaranteeing compliance with all ethical and regulatory standards and ensuring the quality and validity of the research.
The research team, through observation, formulates a research question and idea.
In this phase, it is necessary to prepare the documentation, select the study personnel, obtain the necessary approvals (Ethics Committee, Autonomous Communities, and regulatory agencies), and finally, sign the contracts and register the study on the corresponding platforms.
In this phase, all study documents are created (investigator’s file, recruitment materials, among others), and the data collection notebook is developed. Logistic and coordination tasks are carried out to implement the study. Finally, the initiation visit is conducted, during which all key points of the project are reviewed.
The search and selection of participants are carried out. Study procedures are performed (obtaining informed consent, scheduling study visits, and conducting and tracking procedures). The study is monitored to ensure compliance with regulations and adherence to the research protocol. After its conclusion, the closing visit is conducted.
Data exports are carried out for analysis purposes. These are interpreted in order to address the hypotheses and objectives outlined in the protocol’s design. Finally, the results of the questions posed and the conclusions drawn are documented.
Based on the evidence found, the results are published in scientific journals and specialized conferences to enhance the knowledge of the scientific community.
Our success lies in the combined efforts from the CRO and CTU teams that provide thorough support to the research team.
What do they think of us?
A truly good service, with close communication between the promoter and the CRO, but also independence in carrying out delegated tasks.
The level of satisfaction obtained by different promoters regarding the work carried out by ScienHub Research Support – CTU is 4.66 out of 5.
Check out some of the latest projects we’ve worked on.
The CRO initiates a new study in collaboration with Cardialysis (a leading organization in cardiovascular research focused exclusively on cardiology). Currently, the CRO manages 6 studies in coordination with Cardialysis CRO, located in Rotterdam. The CRO is responsible for handling bureaucratic procedures and monitoring at participating centers in Spain.
The PAX clinical trial has concluded, in which plasma exchange therapy was studied for its effectiveness in improving symptoms of Long COVID. The trial, made possible by Grifols, began in September 2022 and concluded in June 2023. A total of 50 participants were enrolled. The trial was implemented and managed by the CTU and CRO, successfully concluding according to the planned schedule.
Currently, the CRO provides management support for 4 clinical trials in Spain for the International Network for Strategic Initiatives in Global HIV Trials (INSIGHT). The University of Minnesota is the sponsor of these clinical trials, with European coordination conducted by the Centre of Excellence for Health, Immunity, and Infection (CHIP) in Copenhagen. The CRO is responsible for handling bureaucratic procedures and monitoring at participating centers in Spain.