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11:41:13","影片長度":"00:02:09","會議時間":"2024-06-04T09:00:00+08:00","會議名稱":"第11屆第1會期第16次會議（事由：一、行政院院長報告施政方針並備質詢(5月31日)。\n二、討論事項：本院社會福利及衛生環境委員會報告併案審查行政院函請審議、委員邱議瑩等25人擬具「再生醫療法草案」、委員謝衣鳯等19人擬具「再生醫療發展法草案」、委員羅廷瑋等21人、委員黃秀芳等18人、委員王正旭等20人、台灣民眾黨黨團、委員陳菁徽等19人及委員楊瓊瓔等25人分別擬具「再生醫療法草案」等5案(6月4日)。\n三、5月31日上午9時至10時為國是論壇時間。\n四、本次會議不處理臨時提案。）","date":"2024-06-04","start_time":"2024-06-04T11:39:04+08:00","end_time":"2024-06-04T11:41:13+08:00","duration":129,"meet":{"tmpMeeting":null,"title":"立法院第11屆第1會期第16次會議","id":"院會-11-1-16","type":"院會","term":11,"sessionPeriod":1,"sessionTimes":16},"features":["ai-transcript","gazette"],"type":"Clip","gazette":{"lineno":187,"blocks":[["謝委員衣鳯：（11時39分）院長、本院同仁。根據國際再生醫療聯盟（ARM）的統計，2023年全球再生醫療的藥廠進行臨床一期、臨床二期、臨床三期的試驗案件有1,839件，在臺灣目前以特管辦法總核准包含自體免疫細胞、脂肪幹細胞、纖維母細胞等53項適應症項目，截至2023年12月底止，超過70家醫療院所以及20家細胞治療公司，共提出502件申請案，核准258件細胞治療技術，總收案人數達1,398人，可見再生醫療藥品的發展，不管是國內外都非常地快速，需要再生醫療製劑專法，對於藥品製造、運銷、上市後的安全監控、藥品追溯、追蹤都有規範，以確保再生醫療製劑的品質安全跟有效性，來維護病人的醫療權益。","今天再生醫療專法的通過，不只提供醫生、病人武器來對抗罕、重症，也讓我們的衛福部可以依法管理再生醫療的產業，保障病人的權益，也期許未來臺灣的生技產業能夠像半導體產業一樣，成為下一個半導體產業，來促進臺灣的經濟發展。謝謝大家！"],["主席：謝謝謝衣鳯委員的發言。","接下來請登記第8號蘇清泉委員發言。"]],"agenda":{"page_end":570,"meet_id":"院會-11-1-16","speakers":["韓國瑜","邱議瑩","羅廷瑋","楊瓊瓔","王正旭","黃秀芳","劉建國","謝衣鳯","蘇清泉","林月琴","林楚茵"],"page_start":388,"meetingDate":["2024-06-04"],"gazette_id":"1135101","agenda_lcidc_ids":["1135101_00005","1135101_00006","1135101_00007"],"meet_name":"立法院第11屆第1會期第16次會議紀錄","content":"再生醫療製劑條例─ 完成三讀─","agenda_id":"1135101_00005"}},"transcript":{"id":"153491","pyannote":{"name":"ronny","tool":"pyannote","data":{"url":"https://ivod.ly.gov.tw/Play/Clip/1M/153491","tool":"pyannote","id":"153491-pyannote"},"job_id":"SXqNWTX5Gg3WlJxf","queued_at":"2024-06-04 12:01:51","status":"done","log":[{"time":"2024-06-04 12:01:51","msg":"downloading https://ivod.ly.gov.tw/Play/Clip/1M/153491"},{"time":"2024-06-04 12:01:52","msg":"downloading https://ivod-lyvod.cdn.hinet.net/vod_1/_definst_/mp4:1MClips/f4eef9f9bd62cc075f4514e659b9ac02b566fe1f8cd5cc06ae63c9141657ad190687e508e571daec5ea18f28b6918d91.mp4/playlist.m3u8"},{"time":"2024-06-04 12:01:57","msg":"converting mp4 to wav"},{"time":"2024-06-04 12:01:58","msg":"running pyannote"},{"time":"2024-06-04 12:02:04","msg":"status: 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00:01:09,545\n超過70家醫療院所以及20家細胞治療公司共提出502件的申請案合準258件細胞治療技術總收案人數達1398人可見再生醫療藥品的發展不管是國內外都非常的快速需要再生醫療製劑專法\n\n4\n00:01:11,486 --> 00:01:36,847\n對於醫藥品製造、運銷、上市後的安全監控、藥品追溯、追蹤都有規範以確保再生醫療製劑的品質、安全跟有效性來維護病人的醫療權益今天再生醫療專法的通過不只提供醫生、病人武器來對抗罕重症\n\n5\n00:01:37,668 --> 00:01:56,075\n也讓我們的衛福部可以依法管理再生醫療的產業保障病人的權益也期許未來台灣的生技產業能夠像半導體產業一樣成為下一個半導體產業來促進台灣的經濟發展謝謝大家\n\n6\n00:02:04,566 --> 00:02:07,010\n謝謝謝衣鳯委員的發言接下來請登記第8號蘇清\n\n","tsv":"start\tend\ttext\n12557\t18839\t院長、本院同仁根據國際再生醫療聯盟 的統計2023年全球再生醫療的藥廠進行臨床一期、臨床二期、臨床三期的試驗案件有1839件\n29282\t37368\t在臺灣目前以特管辦法總核准包含肢體免疫細胞、脂肪幹細胞、纖維母細胞等53項適應症項目截至2023年12月抵制\n44213\t69545\t超過70家醫療院所以及20家細胞治療公司共提出502件的申請案合準258件細胞治療技術總收案人數達1398人可見再生醫療藥品的發展不管是國內外都非常的快速需要再生醫療製劑專法\n71486\t96847\t對於醫藥品製造、運銷、上市後的安全監控、藥品追溯、追蹤都有規範以確保再生醫療製劑的品質、安全跟有效性來維護病人的醫療權益今天再生醫療專法的通過不只提供醫生、病人武器來對抗罕重症\n97668\t116075\t也讓我們的衛福部可以依法管理再生醫療的產業保障病人的權益也期許未來台灣的生技產業能夠像半導體產業一樣成為下一個半導體產業來促進台灣的經濟發展謝謝大家\n124566\t127010\t謝謝謝衣鳯委員的發言接下來請登記第8號蘇清\n","txt":"院長、本院同仁根據國際再生醫療聯盟 的統計2023年全球再生醫療的藥廠進行臨床一期、臨床二期、臨床三期的試驗案件有1839件\n在臺灣目前以特管辦法總核准包含肢體免疫細胞、脂肪幹細胞、纖維母細胞等53項適應症項目截至2023年12月抵制\n超過70家醫療院所以及20家細胞治療公司共提出502件的申請案合準258件細胞治療技術總收案人數達1398人可見再生醫療藥品的發展不管是國內外都非常的快速需要再生醫療製劑專法\n對於醫藥品製造、運銷、上市後的安全監控、藥品追溯、追蹤都有規範以確保再生醫療製劑的品質、安全跟有效性來維護病人的醫療權益今天再生醫療專法的通過不只提供醫生、病人武器來對抗罕重症\n也讓我們的衛福部可以依法管理再生醫療的產業保障病人的權益也期許未來台灣的生技產業能夠像半導體產業一樣成為下一個半導體產業來促進台灣的經濟發展謝謝大家\n謝謝謝衣鳯委員的發言接下來請登記第8號蘇清\n","vtt":"WEBVTT\n\n00:12.557 --> 00:18.839\n院長、本院同仁根據國際再生醫療聯盟的統計2023年全球再生醫療的藥廠進行臨床一期、臨床二期、臨床三期的試驗案件有1839件\n\n00:29.282 --> 00:37.368\n在臺灣目前以特管辦法總核准包含肢體免疫細胞、脂肪幹細胞、纖維母細胞等53項適應症項目截至2023年12月抵制\n\n00:44.213 --> 01:09.545\n超過70家醫療院所以及20家細胞治療公司共提出502件的申請案合準258件細胞治療技術總收案人數達1398人可見再生醫療藥品的發展不管是國內外都非常的快速需要再生醫療製劑專法\n\n01:11.486 --> 01:36.847\n對於醫藥品製造、運銷、上市後的安全監控、藥品追溯、追蹤都有規範以確保再生醫療製劑的品質、安全跟有效性來維護病人的醫療權益今天再生醫療專法的通過不只提供醫生、病人武器來對抗罕重症\n\n01:37.668 --> 01:56.075\n也讓我們的衛福部可以依法管理再生醫療的產業保障病人的權益也期許未來台灣的生技產業能夠像半導體產業一樣成為下一個半導體產業來促進台灣的經濟發展謝謝大家\n\n02:04.566 --> 02:07.010\n謝謝謝衣鳯委員的發言接下來請登記第8號蘇清\n\n","segments":[{"start":12.557,"end":18.839,"text":"院長、本院同仁根據國際再生醫療聯盟 的統計2023年全球再生醫療的藥廠進行臨床一期、臨床二期、臨床三期的試驗案件有1839件"},{"start":29.282,"end":37.368,"text":"在臺灣目前以特管辦法總核准包含肢體免疫細胞、脂肪幹細胞、纖維母細胞等53項適應症項目截至2023年12月抵制"},{"start":44.213,"end":69.545,"text":"超過70家醫療院所以及20家細胞治療公司共提出502件的申請案合準258件細胞治療技術總收案人數達1398人可見再生醫療藥品的發展不管是國內外都非常的快速需要再生醫療製劑專法"},{"start":71.486,"end":96.847,"text":"對於醫藥品製造、運銷、上市後的安全監控、藥品追溯、追蹤都有規範以確保再生醫療製劑的品質、安全跟有效性來維護病人的醫療權益今天再生醫療專法的通過不只提供醫生、病人武器來對抗罕重症"},{"start":97.668,"end":116.075,"text":"也讓我們的衛福部可以依法管理再生醫療的產業保障病人的權益也期許未來台灣的生技產業能夠像半導體產業一樣成為下一個半導體產業來促進台灣的經濟發展謝謝大家"},{"start":124.566,"end":127.01,"text":"謝謝謝衣鳯委員的發言接下來請登記第8號蘇清"}]}}}}