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題名:臺美醫藥緊急使用授權法制分析與比較
書刊名:興大法學
作者:張愷致
作者(外文):Chang, Kai-chih
出版日期:2022
卷期:31
頁次:頁107-206
主題關鍵詞:緊急使用授權公共衛生緊急事件專案核准特定藥物之製造或輸入藥事法第48條之2醫療器材管理法第35條Emergency use authorizationPublic health emergencyPharmaceutical Affairs ActMedical Devices ActRegulations for approval of specific medical products' manufacturing or importing as a special case
原始連結:連回原系統網址new window
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  • 被引用次數被引用次數:期刊(0) 博士論文(0) 專書(0) 專書論文(0)
  • 排除自我引用排除自我引用:0
  • 共同引用共同引用:9
  • 點閱點閱:1
期刊論文
1.廖建瑜(20110800)。藥品OFF-LABEL USE之管制--以美國與臺灣為例。法學新論,31,37-64。new window  延伸查詢new window
2.廖建瑜(20111000)。藥品OFF-LABEL USE之管制--以美國與臺灣為例。法學新論,32,45-71。new window  延伸查詢new window
3.唐淑美、顏上詠、陳祖裕、林正介(20101200)。受試者保護與人體試驗委員會。醫事法學,17(2),1-12。new window  延伸查詢new window
4.林誠二(20101000)。人體試驗與雙效理論之探討。法令月刊,61(10),75-91。new window  延伸查詢new window
5.陳怡安(20020300)。受試者保護與人體試驗的規範。律師雜誌,270,30-43。  延伸查詢new window
6.Darrow, Jonathan J.、Sarpatwari, Ameet、Avorn, Jerry、Kesselheim, Aaron S.(2015)。Practical, Legal, and Ethical Issues in Expanded Access to Investigational Drugs。New England Journal of Medicine,372(3),279-286。  new window
7.Maher, Carmen、Lushniak, Boris D.(2009)。Availability of medical countermeasures for bioterrorism events: US legal and regulatory options。Clinical Pharmacology & Therapeutics,85(6),669-671。  new window
8.林欣柔、鄒孟珍(20161000)。成全病人的最後一線生機?--擴大近用試驗中藥品之倫理考量及法律挑戰。萬國法律,209,55-63。  延伸查詢new window
9.Krause, Philip R.、Gruber, Marion F.(2020)。Emergency Use Authorization of Covid Vaccines--Safety and Efficacy Follow-up Considerations。The New England Journal of Medicine,383(19)。  new window
10.Petersen, Michael Bang、Bor, Alexander、Jørgensen, Frederik、Lindholt, Marie Fly(2021)。Transparent communication about negative features of COVID-19 vaccines decreases acceptance but increases trust。Proceedings of the National Academy of Sciences,118(29)。  new window
11.Kels, Charles G.(2015)。Dispensing Medical Countermeasures: Emergency Use Authorities and Liability Protections。Health Security,13(2),139-151。  new window
12.Walsh, Daniel(2021)。COVID-19: A Crisis and an Opportunity to Improve the Emergency Use Authorization Process。Minnesota Journal of Law, Science & Technology,22(2),169-220。  new window
13.Mello, Michelle M.、Frakes, Michael D.、Blumenkranz, Erik、Studdert, David M.(2020)。Malpractice Liability and Health Care Quality: A Review。JAMA,323(4),352-366。  new window
14.Thomson, Kyle、Nachlis, Herschel(20200831)。Emergency Use Authorizations During the COVID-19 Pandemic: Lessons From Hydroxychloroquine for Vaccine Authorization and Approval。The Journal of the American Medical Association,324(13),1282-1283。  new window
15.Jarow, Jonathan P.、Lemery, Steven、Bugin, Kevin、Khozin, Sean、Moscicki, Richard(2016)。Expanded Access of Investigational Drugs: The Experience of the Center of Drug Evaluation and Research Over a 10-Year Period。Therapeutic Innovation & Regulatory Science,50(6),705-709。  new window
16.蘇嘉瑞、張楊全、楊弘仁(20111100)。兼顧「權益保護」與「研究促進」--人體試驗委員會的有效運作與法律規範。臺灣醫界,54(11),45-50。  延伸查詢new window
17.謝文哲(20210614)。【全台三級警戒】鴻海洽購BNT進法律商談階段 陳時中曝郭台銘開1條件。鏡周刊。  延伸查詢new window
18.Annas, George J.(2002)。Bioterrorism, public health, and human rights。Health Affairs,21(6),94-97。  new window
19.Binzer, Peggy(2008)。The PREP Act: Liability Protection for Medical Countermeasure Development, Distribution, and Administration。Biosecurity and Bioterrorism,6(4),293-298。  new window
20.Blanchard, Janice C.、Haywood, Yolanda、Stein, Bradley D.、Tanielian, Terri L.、Stoto, Michael、Lurie, Nicole(2005)。In Their Own Words: Lessons Learned From Those Exposed to Anthrax。American Journal of Public Health,95(3),489-495。  new window
21.Burgessa, David C.、Burgessbc, Margaret A.、Leask, Julie(2006)。The MMR vaccination and autism controversy in United Kingdom 1998-2005: Inevitable community outrage or a failure of risk communication?。Vaccine,24(18),3921-3928。  new window
22.Copper, Brian Kurt(2007)。"High and Dry?" The Public Readiness and Emergency Preparedness Act and Liability Protection for Pharmaceutical Manufacturers。Journal of Health Law,40(1)。  new window
23.Courtney, Brooke、Sherman, Susan、Penn, Matthew(2013)。Federal Legal Preparedness Tools for Facilitating Medical Countermeasure Use during Public Health Emergencies。The Journal of Law, Medicine & Ethics,41(S1),22-27。  new window
24.Drew, Liam(2019)。The case for mandatory vaccination。NATURE,575(7784),S58-S60。  new window
25.(2020)。COVID vaccine confidence requires radical transparency。NATURE,586(7827)。  new window
26.Finkelstein, Paige E.(2015)。Expanded Access to Investigational Drugs: What Physicians and the Public Need to Know about FDA and Corporate Processes。AMA Journal of Ethics,17(12),1142-1146。  new window
27.Fountzilas, Elena、Said, Rabih、Tsimberidou, Apostolia M.(2018)。Expanded access to investigational drugs: balancing patient safety with potential therapeutic benefits。Expert Opinion on Investigational Drugs,27(2),155-162。  new window
28.Freimuth, Vicki S.、Quinn, Sandra C.、Thomas, Stephen B.、Cole, Galen、Zook, Eric、Duncan, Ted(2001)。African American's views on research and the Tuskegee syphilis study。Social Science & Medicine,52(5),797-808。  new window
29.Guidry, Jeanine P. D.、Laestadius, Linnea I.、Vraga, Emily K.、Miller, Carrie A.、Perrin, Paul B.、Burton, Candace W.、Ryan, Mark、Fuemmeler, Bernard F.、Carlyle, Kellie E.(2021)。Willingness to get the COVID-19 vaccine with and without emergency use authorization。American Journal of Infection Control,49(2),137-142。  new window
30.Hoffman, Sharona、Goodman, Richard A.、Stier, Daniel D.(2009)。Law, Liability, and Public Health Emergencies。Disaster Medicine and Public Health Preparedness,3(2),117-125。  new window
31.Jarow, Jonathan P.、Lurie, Peter、Ikenberry, Sarah Crowley、Lemery, Steven(2017)。Overview of FDA's Expanded Access Program for Investigational Drugs。Therapeutic Innovation & Regulatory Science,51(2),177-179。  new window
32.Leask, Julie(2002)。Vaccination and risk communication: summary of a workshop, Arlington Virginia, USA, 5-6 October 2000。Journal of Paediatrics and Child Health,38(2),124-128。  new window
33.Liu, Brooke Fisher、Quinn, Sandra C.、Egnoto, Michael、Freimuth, Vicki、Boonchaisri, Natalie(2017)。Public Understanding of Medical Countermeasures。Health Security,15(2),194-206。  new window
34.Mack, George S.(2009)。Expanded Access Rules Pose Quandary for Drug Developers。Nature Biotechnology,27(10),871-872。  new window
35.Marino, Angela(2005)。The Cost of a Countermeasure: The Expansive Liability Protection of the Public Readiness and Emergency Preparedness Act of 2005。University of Florida Journal of Law & Public Policy,20(2),199-220。  new window
36.Martinez, William Chanes(2021)。How to Get Away with Immunity: FDA's Emergency Use Authorization Scheme and PREP Act Liability Protection in the Context of COVID-19。Loyola Consumer Law Review,33(1)。  new window
37.Mayer, Lincoln(2007)。Immunity for Immunizations: Tort Liability, Biodefense, and Bioshield II。Stanford Law Review,59(6),1753-1790。  new window
38.McKee, Amy E.、Markon, André O.、Chan-Tack, Kirk M.、Lurie, Peter(2017)。How Often Are Drugs Made Available Under the Food and Drug Administration's Expanded Access Process Approved?。Journal of Clinical Pharmacology,57(S10),S136-S142。  new window
39.Moulton, Anthony D.、Gottfried, Richard N.、Goodman, Richard A.、Murphy, Anne M.、Rawson, Raymond D.(2003)。What Is Public Health Legal Preparedness?。The Journal of Law Medicine & Ethics,31(4),672-683。  new window
40.Nightingale, Stuart L.、Prasher, Joanna M.、Simonson, Stewart(2007)。Emergency Use Authorization (EUA) to Enable Use of Needed Products in Civilian and Military Emergencies, United States。Emerging Infectious Diseases,13(7),1046-1051。  new window
41.Paek, Hye-Jin、Hilyard, Karen、Freimuth, Vicki S.、Barge, J. Kevin、Mindlin, Michele(2008)。Public support for government actions during a flu pandemic: Lessons learned from a statewide survey。Health Promotion Practice,9(4 Suppl.),60S-72S。  new window
42.Quinn, Sandra Crouse(2008)。Crisis and emergency risk communication in a pandemic: a model for building capacity and resilience of minority communities。Health Promotion Practice,9(4 Suppl),18S-25S。  new window
43.Quinn, Sandra Crouse、Jamison, Amelia M.、Freimuth, Vicki(2021)。Communicating Effectively about Emergency Use Authorization and Vaccines in the COVID-19 Pandemic。American Journal of Public Health,111(3),355-358。  new window
44.Quinn, Sandra Crouse、Kumar, Supriya、Freimuth, Vicki S.、Kidwell, Kelley、Musa, Donald(2009)。Public willingness to take a vaccine or drug under Emergency Use Authorization during the 2009 H1N1 pandemic。Biosecurity and Bioterrorism,7(3),275-290。  new window
45.Quinn, Sandra Crouse、Thomas, Tammy、Kumar, Supriya(2007)。The Anthrax Vaccine and Research: Reactions from Postal Workers and Public Health Professionals。Biosecurity & Bioterrorism,6(4),321-333。  new window
46.Reich, Daniel S.(2003)。Modernizing Local Responses to Public Health Emergencies: Bioterrorism, Epidemics, and the Model State Emergency Health Powers Act。Journal of Contemporary Health Law and Policy,19(2),379-414。  new window
47.Rizk, John G.、Forthal, Donald N.、Kalantar-Zadeh, Kamyar、Mehra, Mandeep R.、Lavie, Carl J.、Rizk, Youssef、Pfeiffer, JoAnn P.、Lewin, John C.(2020)。Expanded Access Programs, Compassionate Drug Use, and Emergency Use Authorizations During the COVID-19 Pandemic。Drug Discovery Today,26(2),593-603。  new window
48.Rubin, G. James、Amlȏt, Richard、Page, Lisa、Wessely, Simon(2009)。Public Perceptions, Anxiety, and Behaviour Change in Relation to the Swine Flu Outbreak: Cross Sectional Telephone Survey。British Medical Journal,339(b2651)。  new window
49.Russell, Philip K.(2007)。Project BioShield: What It Is, Why It Is Needed, and Its Accomplishments So Far。Clinical Infectious Diseases,45(S1),S68-S72。  new window
50.Thomas, Stephen B.、Quinn, Sandra C.(1991)。The Tuskegee Syphilis Study, 1932 to 1972: Implications for HIV Education and AIDS Risk Education Programs in the Black Community。American Journal of Public Health,81(11),1498-1505。  new window
51.Winniford, Austin(2009)。Expanding Access to Investigational Drugs for Treatment Use: A Policy Analysis and Legislative Proposal。Health Matrix,19(1),205-246。  new window
52.Cassidy, Christine、Dever, Danielle、Stanbery, Laura、Edelman, Gerald、Dworkin, Lance、Nemunaitis, John(2020)。FDA Efficiency for Approval Process of COVID-19 Therapeutics。Infectious Agents and Cancer,15(1),1-3。  new window
53.Groopman, Jerome(20061210)。The Right to a Trial: Should Dying Patients Have Access to Experimental Drugs?。The New Yorker。  new window
54.(20210602)。國產疫苗拿「緊急授權」標準太寬鬆?一文看懂高端、聯亞生技疫苗保護力、安全性關鍵重點。今周刊。  延伸查詢new window
55.Siegel, Marc(20041101)。Vaccine Poker。The Nation,2004(Nov.)。  new window
56.Petts, Judith、Niemeyer, Simon(2004)。Health Risk Communication and Amplification: Learning from the MMR Vaccination Controversy。Health, Risk & Society,6(1),7-23。  new window
會議論文
1.(2010)。Medical Countermeasures Dispensing: Emergency Use Authorization and the Postal Model, Workshop Summary。Institute of Medicine (US) Forum on Medical and Public Health Preparedness for Catastrophic Events。  new window
圖書
1.何建志(2018)。公費疫苗法制解析與重構:科學不確定性下自主與公衛之平衡。元照。  延伸查詢new window
2.林以璿(20210220)。COVID-19/AZ疫苗緊急授權通過!指揮中心回應來台施打時間。  延伸查詢new window
3.疾病管制署(20210529)。我國疫苗政策兩大原則:由中央政府與原廠簽約採購並統籌分配執行。  延伸查詢new window
其他
1.後疫情關鍵字:整合筆記編輯部(20210705)。COVID-19疫苗政策之法律爭議,https://covid19.nctu.edu.tw/article/10134。  延伸查詢new window
2.中央社(20210803)。BNT疫苗新進度陳時中:下午簽核通過EUA,https://health.udn.com/health/story/121833/5647296。  延伸查詢new window
3.王駿杰(20210607)。藥事法緊急授權法制不備 陽明交大團隊提修法草案建議,https://health.udn.com/health/story/120951/5514404。  延伸查詢new window
4.行政院(20210712)。「三原則兩共識」公私協力達成BNT疫苗洽購 政院:確保疫苗穩定供應 保護國人健康,https://www.ey.gov.tw/Page/9277F759E41CCD91/f60cc186-52bd-491d-9e3f-21e90790fa9c。  延伸查詢new window
5.何豪毅(20210512)。縣市政府可自購疫苗?陳時中點頭:符EUA合法合規即可,https://cnews.com.tw/174210512a02/。  延伸查詢new window
6.吳亮儀(20210505)。莫德納疫苗通過食藥署緊急授權 陳時中:來台時程不變,https://news.ltn.com.tw/news/life/breakingnews/3521923。  延伸查詢new window
7.吳亮儀(20210610)。嬌生疫苗通過我緊急使用授權 BNT僅「有條件通過」,https://news.ltn.com.tw/news/life/breakingnews/3565594。  延伸查詢new window
8.吳亮儀(20210616)。國光、聯亞研發疫苗遭刁難?指揮中心嚴正澄清:標準一致,https://news.ltn.com.tw/news/life/breakingnews/3571712。  延伸查詢new window
9.呂炯昌(20210527)。「疫苗有能力買到!」傅崑萁:政院速開放地方政府買疫苗,https://www.nownews.com/news/5279162。  延伸查詢new window
10.李宗憲(20200122)。武漢肺炎:台灣首例確診者發病後搭機返鄉台叫停武漢雙向旅遊團,https://www.bbc.com/zhongwen/trad/chinese-news-51202545。  延伸查詢new window
11.國家衛生研究院(20200410)。2020年國衛院論壇「台灣新冠肺炎COVID-19疫苗緊急開發策略」專家諮詢會議,https://enews.nhri.org.tw/archives/3381。  延伸查詢new window
12.張茗喧,江慧珺(20210528)。地方政府、企業怎麼買疫苗?指揮中心公布流程,https://www.cna.com.tw/news/firstnews/202105280156.aspx。  延伸查詢new window
13.張聰秋(20210525)。彰化重度熱區 王惠美盼開放企業買疫苗,https://news.ltn.com.tw/news/life/breakingnews/3545325。  延伸查詢new window
14.陳奐宇,許政俊,孟昭權,溫嘉楷(20210621)。疑似注AZ死亡閣添17例 民眾注疫苗意願降低,https://news.pts.org.tw/article/531744。  延伸查詢new window
15.陳郁仁,林炫均(20210618)。蔡政府授權台積電、鴻海 向BNT洽購1000萬劑疫苗,https://tw.news.yahoo.com/%E8%94%A1%E6%94%BF%E5%BA%9C%E6%8E%88%E6%AC%8A%E5%8F%B0%E7%A9%8D%E9%9B%BB-%E9%B4%BB%E6%B5%B7-%E5%90%91bnt%E6%B4%BD%E8%B3%BC1000%E8%90%AC%E5%8A%91%E7%96%AB%E8%8B%97-043904164.html。  new window
16.陳燕珩(20210624)。接種後死亡再添34例 莊人祥稱解剖26例「死因無關疫苗」,https://www.upmedia.mg/news_info.php?SerialNo=116804。  延伸查詢new window
17.曾郡秋(20210610)。EUA標準為國產疫苗護航?食藥署駁:無關高端!是需取得國內AZ抗體數據,https://newtalk.tw/news/view/2021-06-10/587140。  延伸查詢new window
18.葉韋辰(20210616)。獨厚高端?傳國光疫苗因基準不公遭淘汰 指揮中心說話了,https://news.tvbs.com.tw/life/1528941。  延伸查詢new window
19.劉宏恩(20210827)。高端疫苗注射後死亡的因果關係如何認定?,https://forum.ettoday.net/news/2065873#ixzz7B7IMN5DL。  延伸查詢new window
20.劉俊男(20210521)。捐疫苗須通過EUA食藥署:未收到申請,https://news.cts.com.tw/cts/society/202105/202105312044299.html。  延伸查詢new window
21.衛生福利部中藥司(20210519)。衛生福利部核准「臺灣清冠一號濃縮製劑」專案製造,應經中醫師處方,民眾勿自行購買服用,https://www.mohw.gov.tw/cp-16-60830-1.html。  延伸查詢new window
22.衛生福利部食品藥物管理署(2018)。公告第一階段適用藥害救濟法之藥物範圍,藥害救濟法令解釋彙集,https://www.tdrf.org.tw/wp-content/uploads/2019/01/201810-Drug-Injury-Relief-Act.pdf。  延伸查詢new window
23.衛生福利部食品藥物管理署(20210501)。新型冠狀病毒檢驗試劑申請專案製造相關資訊,https://www.fda.gov.tw/TC/siteContent.aspx?sid=11671。  延伸查詢new window
24.衛生福利部食品藥物管理署(20210610)。食藥署廣納並參考專家意見,訂定國產COVID-19疫苗緊急使用授權審查標準,透過嚴謹審查確保疫苗品質安全有效,https://www.mohw.gov.tw/cp-16-61305-1.html。  延伸查詢new window
25.衛生福利部疾病管制署。嚴重特殊傳染性肺炎,https://www.cdc.gov.tw/Disease/SubIndex/N6XvFa1YP9CXYdB0kNSA9A。  延伸查詢new window
26.韓婷婷(20210615)。高端公告 已向衛福部申請疫苗緊急使用授權,https://www.cna.com.tw/news/firstnews/202106150316.aspx。  延伸查詢new window
27.(20210325)。AZD1222 US Phase III primary analysis confirms safety and efficacy,https://www.astrazeneca.com/media-centre/press-releases/2021/azd1222-us-phase-iii-primary-analysis-confirms-safety-and-efficacy.html#!。  new window
28.(20200401)。Coronavirus: Greatest test since World War Two, says UN chief,https://www.bbc.com/news/world-52114829。  new window
29.U.S. Government Printing Office(2004)。BioShield II: Responding to an Ever-changing Threat : Joint Hearing Before the Committee on the Judiciary and Committee on Health, Education, Labor, and Pensions, United States Senate, One Hundred Eighth Congress, Second Session, October 6, 2004,https://www.judiciary.senate.gov/meetings/bioshield-ii-responding-to-an-ever-changingthreat。  new window
30.(20191121)。How Low Can They Go? Civil, Tort, Med Mal, Products Caseloads and Jury Trials,https://centerjd.org/content/how-low-can-they-go-civil-tort-med-mal-products-caseloads-and-jury-trials。  new window
31.Kadlec, Robert(20130125)。Renewing the Project BioShield Act: What Has It Bought and Wrought?,https://www.cnas.org/publications/reports/renewing-the-project-bioshield-act-what-has-it-bought-and-wrought。  new window
32.(20210823)。Pfizer-Biontech Covid-19 Vaccine Comirnaty® Receives Full U.S. FDA Approval for Individuals 16 Years and Older,https://www.pfizer.com/news/press-release/press-release-detail/pfizer-biontech-covid-19-vaccine-comirnatyr-receives-full。  new window
33.Rapaport, Lisa(20150929)。U.S. 'Right to Try' Laws May Not Help Dying Get Unapproved Drugs,https://www.reuters.com/article/us-health-dying-experimental-drugs-idUSKCN0RS2LN20150928。  new window
34.Ridwan, Raiiq(20200520)。Remdesivir and COVID-19: Justified in Emergency Use Authorization?,https://www.authorea.com/users/324516/articles/452684-remdesivir-and-covid-19-justified-in-emergency-use-authorization。  new window
35.(20200813)。'This is the greatest public health crisis to hit this nation in a century': US CDC director,https://tbsnews.net/coronavirus-chronicle/greatest-publichealth-crisis-hit-nation-century-us-cdc-director-119023。  new window
36.United States Department of Health and Human Services(20200131)。Determination that a Public Health Emergency Exists Nationwide as the Result of the 2019 Novel Coronavirus,https://www.phe.gov/emergency/news/healthactions/phe/Pages/2019-nCoV.aspx。  new window
37.U.S. Food & Drug Admin。Emergency Use Authorization for Vaccines Explained,https://www.fda.gov/vaccines-blood-biologics/vaccines/emergency-use-authorization-vaccines-explained。  new window
38.U.S. Food and Drug Administration(2017)。Emergency Use Authorization of Medical Products and Related Authorities,https://www.fda.gov/media/97321/download。  new window
39.U.S. Food and Drug Administration。Expanded Access for Medical Devices,https://www.fda.gov/medical-devices/investigational-device-exemption-ide/expanded-access-medical-devices。  new window
40.U.S. Food and Drug Administration(2017)。Expanded Access to Investigational Drugs for Treatment Use--Questions and Answers: Guidance for Industry,https://www.fda.gov/regulatory-information/search-fda-guidance-documents/expanded-access-investigational-drugs-treatment-use-questions-and-answers。  new window
41.(20210823)。FDA Approves First COVID-19 Vaccine,https://www.fda.gov/news-events/press-announcements/fda-approves-first-covid-19-vaccine。  new window
42.U.S. Food and Drug Administration(2017)。Format and Content of a REMS Document Guidance for Industry,https://www.fda.gov/media/77846/download。  new window
43.U.S. Food and Drug Administration。Frequently Asked Questions (FAQs) about REMS,https://www.fda.gov/drugs/risk-evaluation-and-mitigation-strategies-rems/frequently-asked-questions-faqs-about-rems。  new window
44.U.S. Food and Drug Administration。Risk Evaluation and Mitigation Strategies,https://www.fda.gov/drugs/drug-safety-and-availability/risk-evaluation-and-mitigation-strategies-rems。  new window
45.Wamsley, Laurel(20201022)。Researchers Find Doubts About COVID-19 Vaccine Among People Of Color,https://www.npr.org/sections/coronavirus-live-updates/2020/10/22/926813331/researchersfind-doubts-about-covid-19-vaccineamong-people-of-color。  new window
46.Werner, Michael J.,Klock, Sara M.。PREP Act: Liability Protection Is Available During COVID-19 Pandemic,https://www.hklaw.com/en/insights/publications/2020/05/prep-act-liability-protection-is-available-during-covid19-pandemic。  new window
47.吳亮賢(20210615)。又不公開會議記錄!時力批國產疫苗EUA審查標準黑箱,https://udn.com/news/story/122190/5533292。  延伸查詢new window
48.侯俐安(20211019)。記者疫苗嚴重不良反應認定模糊 陳時中允一個月修正,https://udn.com/news/story/122190/5827185。  延伸查詢new window
49.(20210624)。打疫苗169人逝 台中市增4例共34死最多!台北增8例共17死,https://tw.appledaily.com/life/20210624/6LPFJOPW6REC5PFL4DXLRE42ME/。  延伸查詢new window
50.張君堯(20190616)。美新研究:新冠病毒早在2019年12月中就在美國出現,https://udn.com/news/story/121707/5535356。  延伸查詢new window
51.郭政芬,陳雨鑫,邱宜君(20200414)。快篩難行卡在3關鍵,https://udn.com/news/story/120940/4489781。  延伸查詢new window
52.陳雨鑫(20200529)。台灣新冠試劑研發錯過最佳時機 專家提三點補救方案,https://udn.com/news/story/120940/4599823。  延伸查詢new window
53.陳惠玲(20210624)。AZ疫苗接種意願低 汐止75歲施打率剩2成5,https://udn.com/news/story/7323/5555721。  延伸查詢new window
54.陳熙文(20210618)。不只授權郭台銘 政院宣布台積電、永齡代表政府洽購1000萬劑疫苗,https://udn.com/news/story/122190/5541215。  延伸查詢new window
55.楊喻斐,林巧雁(20210615)。郭台銘買疫苗露曙光永齡已接獲有條件專案進口許可函,https://tw.appledaily.com/property/20210615/MH66XF64FRHT5DPYGOQ6FVFFWA/。  延伸查詢new window
56.鍾兆馨(20210624)。疫苗後死亡 速設EUA藥害補償基金,https://udn.com/news/story/7339/5553693。  延伸查詢new window
57.蘇南(20210620)。接種後死亡誰該負責?如何求償?新冠疫苗的法律風險,https://tw.appledaily.com/forum/20210620/JPPGHXT64BHQJPE3MYBILJUXTY/。  延伸查詢new window
圖書論文
1.Quinn, Sandra Crouse、Thomas, Tammy、McAllister, Carol(2008)。Lessons from the 2001 Anthrax Attack: A Conceptual Model for Crisis and Emergency Risk Communication。Crisis Communication And The Public Health。  new window
 
 
 
 
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