CROPHA PROJECT & TRIAL DEVELOPMENT
With our many years' experience in clinical research, CROPHA is able to assist customers with the full or partial organization, development and management of clinical trial projects (full service is limited to phase I and II trials), either in Belgium or the country of your choice. These trials can be coordinated at a single site or several according to the product needs and on the location of key participating physicians.
Specific competences include:
- REGULATORY
- MEDICAL WRITING
- DRUG PACKAGING/ LABELING
- CLINICAL MONITORING
- PROJECT MANAGEMENT
- DATA MANAGEMENT
- CALL CENTER FOR PATIENT RECRUITMENT
- BIOSTATISTICS
- FEASIBILITY STUDIES
- NOTICE READABILITY STUDIES
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