CFDA issued relevant Requirements on Strengthening Supervision and Management of Pharmaceutical Excipients
The China Food and Drug Administration (CFDA) issued the Relevant Requirements on Strengthening Supervision and Management of Pharmaceutical Excipients. The Requirements specifies the respective responsibilities of drug manufactures, pharmaceutical excipients manufactures, and drug regulatory departments; defines the supervision mode for pharmaceutical excipients; establishes the work mechanisms including information publicity, supervision extension and social supervision; and intensifies the attack to violations of laws and regulations. The Requirements will come into effect as of February 1, 2013.
Information source: http://www.sfda.gov.cn/WS01/CL0051/73960.html
