International Program for site staff conducting clinical research
Category
- Clinical Trial Management
- Topic: Site Management
- Short Description: 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: 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 This training has been developed out of Europe, so special attention must be taken to GDPR compliance.
- Provider: Society for Clinical Research Sites
- Level: Beginner
- Language: English/Mandarin
- Cost: Free
- Format: On-line modules
- Duration: 5 hours
- Certificate: No
- Link