On Site Monitoring

Our study coordinators and sub-researchers are in charge of monitoring and managing the control during the monitoring visits of the sponsors. During the visits are available for any questions and clarification of what emerged during the monitoring, as well as for feasibility visits, start and closure of studies.

Data Management

Our data staff have significant experience in entering data and filling in case report forms (CRFs) and other platforms. The equipment guarantees high integrity and accuracy of data collection. Our data personnel operate in full compliance with all applicable regulations, including GCP and certificates on CFR platforms.

Quality Assurance

Our quality assurance team ensures that all trials are carried out to the highest quality standards in accordance with good clinical practice (GCP) guidelines, protocols and regulatory requirements. This guarantees trial patients that their rights, safety and well-being are protected. Some of the services that guarantee the quality of the center include internal audits, calibrations to medical teams and periodic review of facilities. The team also supports site staff in certifications, training and preparation for research protocols.

Planning Studies

Each new project or application will be followed by our business operations. VRI strives to understand the requirements of the project and adapts the proposal to meet the objectives of its client and / or supplier.