- Quality and Safety: Medicines > Quality Assurance
- Quality and Safety: Medicines > Safety and Efficacy
(1995; 36 pages) [French] [Spanish]
6.4 Data management
The monitor should assist the investigator in reporting the data and results of the trial to the sponsor, e.g. by providing guidance on correct procedures for completion of case-report forms (CRFs), and by verifying the accuracy of data obtained (see also Section 8).