Within the scope of the Regulation on Clinical Trials of Medicinal Products for Human Use, Guideline on the Definition of Investigational Products and the Use of Auxiliary Medicinal Products for Human Use and Guideline on the Quality Requirements of Biological Products Used in Clinical Trials Were Drafted
1 Feb 2024
Within the scope of the Regulation on Clinical Trials of Medicinal Products for Human Use published in the Official Gazette dated 27/05/2023 and numbered 32203, the Draft Guideline on the Definition of Investigational Products and on the Use of […]