What you will learn
- How to comply with ICH-GCP and other clinical trial related regulations and guidelines, when working within clinical development (good clinical practice)
- How to understand potential inspection findings in relation to the revised ICH-GCP guideline (R2)
What your company will get
- A GCP professional who is updated and knows the essence of current ICH-GCP and how to ensure compliance
- A GCP professional who has focus on potential inspection findings in relation to the revised ICH-GCP guideline (R2)
- A GCP professional who, with respect to ICH-GCP, can provide valuable input to all other team members within a Clinical Research Unit