Clinical Research Monitoring
Ensuring quality and compliance to your clinical research monitoring.
Eurotrials clinical research monitoring professionals identify the best sites for your study and provide the necessary support for your project to reach the deliverables quickly and complying with all the local and global regulatory requirements. Our qualified teams are located in our two main regions, Europe and Latin America, and receive continuous training to ensure that knowledge of existing legislation and techniques are always up-to-date.
With many years of experience in international, regional and local clinical research monitoring in these two regions, we’ve a large database of qualified sites with access to patients in a variety of therapeutic areas. Our team have built a strong relationship with other professionals at relevant sites, and developed a deep understanding of the challenges that sites are facing. In case you need, e.g. a clinical research monitoring of an orphan drug or an ophthalmologic product, we have the necessary capabilities and focus to ensure you have your product to the market safely and quickly.
- Study Feasibility
- Site Evaluation
- Patient Recruitment, retention support and compliance tracking
- On site monitoring, remote monitoring & site management
- Query management and resolution
- Safety Reporting
- Protocol Deviations Management
- Set up, maintenance & quality check of TMF, Investigator and Pharmacists Site Files
- Regulatory Compliance Monitoring
Eurotrials approach for clinical research monitoring diverge, from on-site monitoring, remote or risk based monitoring. Our professionals are always prepared and trained to monitor any study with the right methodology, with high focus on quality, compliance and cost-efficiency.
Our team structure:
Our clinical operations are developed under the guidance and management of a Project Leader, or Project Manager, which leads CRAs, CTAs, in-house CRAs, seniors or Lead CRAs. Both our CRAs and our Project Leaders are in constant contact with the sponsor.
We can monitor your interventional trial or non-interventional study at a Eurotrials qualified centre or any other centre you want your research to be conducted, from primary health care centres to hospitals and specialized centres.