Active and individual support in the development, implementation and animation of your project
Our Project Manager can take charge of each stage of your study monitoring, ensuring compliance with Good Clinical Practices (ICH) and regulations. He coordinates all operations related to clinical research activities.
Project management and monitoring is carried out by a rigorous project manager and listens to the investigators, providing advice and answers.
Our expertise
Study design
Opening of eCRF access
Study monitoring and data management
Closure of centers
Communication and coordination with all stakeholders in the study
Regulatory submissions for minimal risk observational and interventional studies
Writing of documents related to the study
Development of Newsletters on the progress of the study
