General guidelines
Modifications and comments
The purpose of this course is to define the process followed for designing and reviewing a CRF for a
clinical trial in ClinServ. The CRF design is performed by the Medical Writer (MW) while the CRF
development is performed by the Data Manager (DM) and the CRF review is done by the Lead Medical Writer (LMW) in ClinServ.
0 Reviews
Layal Feghali, Senior Quality Associate at ClinGroup. Responsible for the Quality Management System for units/departments.
