Consultancy and practical information during the preparation of the clinical research project include:

Consultancy on protocol design and methodology
Consultancy on systematic review, meta analysis, and trial sequential analysis
Information on project registration
Information on regulatory and ethical requirements
Information on clinical trial sites and participant recruitment
Information on insurance
Information on cost evaluation and funding opportunities
Information on contracting

Services provided during the conduct of the clinical research project include:

Submission to, and interaction with, competent authorities and ethics committees
Support with insurance contracting
Adverse event reporting
Monitoring
Data management
Project management
Development of central documents and trial master file
Recruitment and evaluation of trial sites
Training of study personnel
Investigational medicinal product management
Blood and tissue samples management

For any further information on consultancy or services, please contact your national European Correspondent