OUR EXPERTISE

Euclid offers full range of clinical trial management activities from study design to reporting to Competent Authorities and dissemination, with the highest standards of quality management systems.

Global expertise

EUCLID offers specialized expertise across key areas of clinical research, combining methodological support, effective trial coordination, robust data management, advanced statistical analysis and dissemination/reporting to meet the needs of international and/or complex studies.

Methodology
From the definition of the design to the dissemination.
Support in project set-up
Support to: develop protocols, grant application, obtain funding, seek ethical and regulatory approval.
Trial Management
Global coordination, site selection and monitoring, project management, GCP, ISO.
Data Management
eCRF, management of multi-dimension databases, data validation and cleaning.
Statistics
Conduct complexe statistical analyses.
Dissemination - Reporting
Report writing and co-writing of publications.

Main research areas

INFECTIOUS DISEASES
VACCINOLOGY / IMMUNOLOGY
CANCER

We are open to other domains that we can handle according to the platform’s capacities.

Specific expertises

Successful experience in the preparation of European calls (Horizon Europe, IHI, EDCTP)
Innovative methods and tailored solutions for trial design, from early to confirmatory phases
Methodological development for complex clinical trials (e.g., platform trials, adaptive trials)
Strengthening institutional capacities in clinical research for complex/international trials and partners from low-resource countries
The EUCLID platform is particularly sensitive to the capacity in clinical research and good clinical practice (GCP) skills during the conduct of clinical trials.

Capacity Building

We can implement the training needed ensuring that all basic and essential skills required to maintain high quality of trial conduct are covered for all staffs involved in clinical trials. This covers Good Clinical Practice (GCP), Case report Form (CRF) development and data management, quality control, basic epidemiology, risk assessments, pharmacovigilance, research ethics and scientific integrity, communication, project planning.