Page 109 - 2017食品藥物管理署年報(英文版)
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2017 Taiwan Food and Drug Administration Annual Report  Chapter 7. International Cooperation and Cross-strait Exchanges










                        the seminar, which were: “The Regulations and Implementation of the Systematic

                        Inspection for Import Food According to Act Governing Food Safety and Sanitation
                        in Taiwan” and “Introduction of Taiwan food traceability system”.
                     (2) Host “International seminar for food adulteration and Chinese herb misuse” on March

                        29, 2016 and invite experts from the US and UK to Taiwan sharing their opinions
                        regarding such hot topic among international society. Such seminar greatly improves
                        national identification technology, non-specific target analysis and Chinese herbal
                        medicinal products.

                     (3) Host “International seminar for processing aids” on July 29, 2016 and invite experts
                        and industry representatives from New Zealand, EU, USA, China, Japan and Taiwan
                        sharing their opinions regarding laws, management and industrial application of
                        processing aids, and the most updated management regulations as well as experience.

                     (4) Host “International seminar for import food safety management” between September
                        29-30, 2016 and invite food safety officials from Austria, Hungary and Japan sharing
                        their food management system and boarder inspection measures.

                     (5) Host “2016 International Symposium on Cosmetic Regulation” on August 2, 2016
                        and invite government officials and experts from EU, Association of Southeast Asian
                        Nations (ASEAN), USA, Japan and China to assist representatives of Taiwan’s
                        government, industry and academic sectors in understanding the current regulatory

                        status and future trends of related products.
                     (6) Organize  “International Conference on Medical Device Regulations for

                         Implementation” in Taiwan on August 25, 2016. TFDA invited experts from EU,
                         Canada and USA to address relevant regulation and future perspectives as well as
                         Unique Device Identification (UDI). Additionally, experiences on pre-marketing
                                                                                  review process, post-
                                                                                  marketing surveillance
                                                                                  and UDI printing and
                                                                                  labeling practices were
                                                                                  exchanged (Figure
                                                                                  7-6).





                      Figure 7-6  International Conference on Medical Device Regulations for Implementation








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