Page 45 - 2021 Taiwan Food and Drug Administration Annual Report
P. 45

Section 4                                            working groups to formulate global drug
                                                     technical guidelines to keep up with inter-
Actively Participated in                             national standards and build a regulatory
International Events of                              environment that has international competi-
Medicine                                             tiveness.

Introduction of the Policy                           II. Continued to participate in
                                                        APEC international confer-
    TFDA continues promoting international              ences
cooperation in pharmaceutical products and
actively participating in important interna-             TFDA actively participates in the work
WLRQDO  RUJDQL]DWLRQ  DFWLYLWLHV   VXFK  DV  WKH     promoted by the APEC Regulatory Harmoni-
$VLD  3DFL¿F (FRQRPLF &RRSHUDWLRQ  $3(&              ]DWLRQ 6WHHULQJ &RPPLWWHH  5+6&   DQG DFWV 
and The International Council for Harmon-            as a leading economy in promoting “Good
isation of Technical Requirements for Phar-          5HJLVWUDWLRQ  0DQDJHPHQW   *50 ´   DQG  UHJ-
PDFHXWLFDOV  IRU  +XPDQ  8VH   ,&+    3KDUPD-        ularly reports the results of GRM promotion
ceutical Inspection Co-operation Scheme              DW $3(&  5+6&  LQWHUQDWLRQDO  FRQIHUHQFHV  
(PIC/S). TFDA is also working to strengthen          which continues to make the country’s voice
bilateral and multilateral cooperation through       heard on the global stage.
interaction and experience sharing with vari-
RXV  LQWHUQDWLRQDO  UHJXODWRU\  LQVWLWXWLRQV   IXU-  III. Conducted the 8th Joint Confer-
ther enhancing our international participation          ence of Taiwan and Japan on
as well as the impact to the world.                     Medical Products Regulation

Implementation Strategy                                  The 8th Joint Conference of Taiwan
                                                     and Japan on Medical Products Regulation
I. Expanded participation in ICH                     ZDV  KHOG  RQ  2FWREHU              'XH  WR  WKH 
   related meetings.                                 &29,'     SDQGHPLF   WHOHFRQIHUHQFLQJ  ZDV 
                                                     FRQGXFWHG  IRU  WKH  ¿UVW  WLPH  ZLWK  WKH  FRQIHU-
    ,Q  UHFHQW  \HDUV  7)'$  KDV  EHHQ  FRP-         ence attendees in Japan. In addition to the
mitted to establishing international drug            government officials from both Japan and
management regulations and promoting the             7DLZDQ   WKHUH  ZHUH  DERXW       SUDFWLWLRQHUV 
harmonization of the country’s drug regu-            from the medicine and medical equipment
lations and ICH guidelines. After officially         industries in Taiwan and Japan attending the
becoming a member of the ICH regulations             conference.
LQ         7)'$  H[SDQGHG  LWV  SDUWLFLSDWLRQ  LQ 
the ICH conference and worked with expert                ,Q  WKH  PHHWLQJ   UHSUHVHQWDWLYHV  IURP 
                                                     Taiwan and Japan shared their experience on

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