Page 47 - 2020Taiwan Food and Drug Administration Annual Report
P. 47

of western medicines and pharmacy operators who have obtained a drug license for western
                     medicine preparations should fulfill the regulations in the “Western Pharmaceuticals Good
                     Distribution Practice Regulations,´ VWDUWLQJ IURP -DQXDU\          7KLV LV WKH ¿UVW VWDJH RI *'3
                     timeline.
                         The Ministry of Health and Welfare continued to implement the second stage of GDP
                     timeline. On May 10, 2019, it was announced that pharmacy operators of western medicine
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                     the “Western Pharmaceuticals Good Distribution Practice Regulations,” starting from January 1,

                     2022.

                     III. Implemented the GDP related supplementary measures
                         TFDA has progressively promoted the distribution and management system of western
                     medicines since 2011 and provided consultation and educational training to the business
                     operators in the industry, including continuing to conduct topic forums, technical seminars, and
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                     TFDA actively communicate with the industry to promote related management policies, and
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                     and announce the GDP regulations to be used as a reference for the business operators.



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                         As of the end of 2019, 691 western pharmaceutical manufacturers and pharmacy operators
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                     the quality of drug storage and transportation as well as the quality and safety of the public’s
                     drugs usage.




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                     Introduction of the Policy
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                     Introduction of the Polic
                         TFDA continues to promote international cooperation in pharmaceutical products in order to
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                     TFDA actively participates in important international organization activities, such as the Asia-
                     Pacific Economic Cooperation (APEC) and The International Council for Harmonisation of
                     Technical Requirements for Pharmaceuticals for Human Use (ICH), Pharmaceutical Inspection
                     Co-operation Scheme (PIC/S) and strive to hold relevant international conferences in Taiwan, to
                     strengthen the bilateral and multilateral cooperation through interaction and experience sharing
                     with international regulatory institutions.

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