Site Management Modules
Category
- Clinical Trial Management
- Topic: Outline of the basic components related to Principal Investigator oversight of clinical trials and the foundational concepts of Clinical Research in accordance with the ICH Guideline for Good Clinical Practice
- Short Description: Principal Investigator Oversight Informational Program, Adverse Events and Safety, Clinical Research Overview, Clinical Practice vs Clinical Research , Conducting a Study , IRB/IEC Responsibilities and Informed Consent, Delegation and Training, Source Documentation, Investigational Product, Essential Documents for a Clinical Study, Facilities and Equipment, Monitoring and Auditing
- Provider: Society for Clinical Research Sites
- Level: Beginner
- Language: English/Mandarin
- Cost: Free
- Format: On-line modules
- Duration: Unknown
- Certificate: No
- Link