Page 42 - 2018食藥署年報(英文版)
P. 42

Electronic Submission

                                                                                 & Online Application
                                                                                 Platform



           Refuse-to-File
           for Drug

           Registration
                                                 Advancement

                                               & Consultation

                                               of Drug Review
                                                      System


                                                                                          Management of
                                                                                          Regenerative
                                                                                          Medicine
           Advancement of
           Pharmaceutical
           Clinical Trial Review
           System

                                                    Consultation

                                               on Medicinal Products






             APEC Regulatory Science Training Center of Excellence


             TFDA Organized the “2017 APEC Good Registration Management (GRM)
             Regulatory Science Center of Excellence Workshop.”











               Policy on     Management          Establish      Good Distri-    Advancement of       PIC/S
             Orphan Drug  Policy on Medicinal   Drug Patent        bution       testing technolo-   Meeting
             Management       Product Trace      Linkage          Practice        gy on illegal
                           and Track System       System           (GDP)             drugs
   37   38   39   40   41   42   43   44   45   46   47