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| Clinical Trial Management |
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Clinical monitoring and site management are conducted by top of the line Clinical Research Associates (CRAs), or monitors, who are knowledgeable of:
- The disease, pathology, protocol, the investigative product.
- Informed consent and written information provided to subjects.
- The sponsor's Standards of Practices, Good Clinical Practices, and the applicable regulatory requirements.
Resources for clinical monitoring and site management are located regionally, based on therapeutic experience and on geographical locations of the investigative sites.
TrialMed has a comprehensive training program provides consistent training in Standard Operating Procedures (SOPs), Good Clinical Practices (GCPs)/International Conference on Harmonization (ICH) Guidelines, and regulatory requirements across regions.
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