ƽ°²Ò¹ÉÇÍ·zotyÖÐÅ·ÌåÓýϲÓTGAÈÏ֤ͨ¹ý
2010Äê12ÔÂ24ÈÕ£¬£¬£¬£¬£¬£¬£¬£¬ÔÚÊ¥µ®Æ½°²Ò¹À´ÁÙǰ£¬£¬£¬£¬£¬£¬£¬£¬¼¯ÍÅ×ܲ¿ÊÕµ½×îºÃµÄÊ¥µ®ÀñÎ¡ªÏÂÊôÉÇÍ·ÊÐzotyÖÐÅ·ÌåÓýÖÆÒ©ÓÐÏÞ¹«Ë¾Í¨¹ý°Ä´óÀûÑÇTGA£¨Therapeutic Goods Administration£©µÄËùÓÐÉóºË£¬£¬£¬£¬£¬£¬£¬£¬Ð§¹ûÇкÏÒªÇ󣬣¬£¬£¬£¬£¬£¬£¬½«ÔÚÊ¥µ®½Úºó·¢·ÅGMPÖ¤ÊéGMPÈÏÖ¤Ö¤Êé (GMP Certificate of Manufacturing Facility)¡£¡£¡£¡£¡£¡£