| Safety Monitoring |
Article Index for Safety |
Website Links For Safety |
Information AboutSafety Monitoring |
| CATEGORIES ABOUT SAFETY MONITORING | |
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Responsibility for data and safety monitoring depends on the phase of the study and may be conducted by sponsor or CRO staff or contractor, and/or by the Principal Clinical Investigator /project manager conducting the study. Regardless of the method used, monitoring must be performed on a regular basis. Oversight of the monitoring activity is the responsibility of the sponsor. FURTHER READING
EXTERNAL LINKS {pharma-stub}} |
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