9 April, 2014    Лондон , Великобритания
Clinical investigation with (newly discovered) drugs involving human subjects is a precarious action and could lead to ethical dilemmas. It is important to know which parties are involved in clinical trials and what their responsibilities are, whilst being aware of the (inter)national laws and regulations. Directives for good clinical practice are recorded in the ICH-Good Clinical Practice (GCP) guideline.

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