Drug Administration Law of the People's Republic of China
date:May 18, 2015
e qualifications of clinical study institutions for drugs shall be formulated jointly by the drug regulatory department and the administrative department for health under the State Council.
When a new drug has gone through clinical trials and passed the evaluation, a New Drug Certificate shall be issued upon approval by the drug regulatory department under the State Council.
Article 30 The institutions for non-clinical safety evaluation and study and clinical study instit
33/117 next page prev page home page last page
go back |  refresh |  WAP home |  Web page version  | login
06/29 03:12