According to Article 17 of the Detailed Rules for the Implementation of the Drug Administration Law: "When applying for clinical trials of new drugs, new drug research units must submit relevant materials and samples in accordance with the provisions of the Measures for the Examination and Approval of New Drugs." Article 18 stipulates: "Clinical trials or clinical verification of new drugs shall be conducted in medical units approved by the health administrative departments of provinces, autonomous regions and municipalities directly under the Central Government." Article 26 of the Law on Medical Practitioners also has relevant provisions: "Doctors should truthfully introduce their illness to patients or their families, but should pay attention to avoid causing adverse consequences to patients. Doctors should carry out experimental clinical medical treatment with the consent of the hospital and the consent of the patient himself or his family. " Therefore, hospitals have no right to try new drugs on patients, especially without the consent of patients, which is illegal.