date:May 18, 2015
he basis of this Law. The drug regulatory department shall inspect a drug manufacturer as to its compliance with the GMP requirements and issue a certificate to the manufacturer passing the inspection.
The specific measures and schedule for implementing the GMP shall be formulated by the drug regulatory department under the State Council.
Article 10 With the exception of the processing of prepared slices of Chinese crude drugs, a drug shall be produced in conformity with