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

Full range of clinical trial management activities from study design to reporting to Competent Authorities and dissemination, following the highest standards of quality and risk management.

Support in project set-up
Support to develop protocols, obtain funding, seek ethical and regulatory approval.
Methodology
from the definition of the design to the dissemination.
Data Management
eCRF, management of multi-dimension databases, data validation and cleaning.
Statistics
Conduct complexes statistical analyses.
Trial Management
Global coordination, site selection and monitoring, project management, GCP, ISO.
Dissemination - Reporting
Support for grant applications, 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
Innovative methods and tailored solutions for trial design, from early to confirmatory phases
Capacity building Ressource‐limited settings
Ressource‐limited settings
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.