Obligations of the administrative agencies to medication use in the field of health law

Implementations of the right to health, which is a social right, are subject to interpretation in the context of obligations imposed on the states parties by the international treaties. In this work, first of all, the obligations of the administrative bodies to offer public health care services were covered. Later, the administrative obligations to medication use, which is the main focus of the study, was assessed based on these three facets: 1) the responsibilities of health care providers during and after a medical treatment in relation to the requirements for medical intervention to be legally compliant, 2) the level of administrative authority on the provision of medications and pharmaceutical clinical trials, and 3) policies and procedures for conducting clinical drug research.