For all short courses a pass mark of 80% is required for certification
Short Courses in Clinical Research:
Introduction to Clinical Research
ICH Good Clinical Practice
This ICH E6 GCP Investigator Site Training meets the Minimum Criteria for ICH GCP Investigator Site Personnel Training identified by TransCelerate BioPharma as necessary to enable mutual recognition of GCP training among trial sponsors.
The Research Question
The Study Protocol: Part one
The Study Protocol: Part two
Data Safety Monitoring Boards for Clinical Trials
Introduction to Informed Consent
Introduction to Data Management For Clinical Research Studies
Introduction to Collecting and Reporting Adverse Events
Specialist Short Courses:
Introduction to Reviewing Genomic Research
The Retrospective Treatment Outcome Study for Traditional Medicines
How to Conduct GCP Inspections/Audits at the Clinical Investigator Site
Introduction to Good Clinical Laboratory Practice
Ethics of Ancillary Care in Research
Ethics and Best Practices in Sharing Individual-Level Research Data
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