The objective of ICH-GCP guidelines is to provide a unified standard for the European Union (EU), Japan and the United States to facilitate the mutual acceptance of clinical data by the regulatory authorities in these regions. This workshop will bring you to a high level of preparation necessary to carry out clinical trials according to the principles of ICH-GCP.
This workshop is designed for physicians, study nurses, study managers, monitors and anyone who is involved in clinical trials.
Please contact us to find out out when is the first available workshop date.
Our experts will gladly advice you personally. We look forward to your call or your message.