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Кто решает вопрос о допуске вакцины для самых маленьких
Европейское агентство по лекарственным средствам (EMA) в настоящее время рассматривает вопрос об одобрении антиковидной вакцины производителей BioNTech и Pfizer для детей в возрасте от пяти до одиннадцати лет! Об этом ЕМА объявило 18 октября в Амстердаме.
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Кто решает вопрос о допуске вакцины для самых маленьких
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25.11.2021 | www.kla.tv/20704
Европейское агентство по лекарственным средствам (EMA) в настоящее время рассматривает вопрос об одобрении антиковидной вакцины производителей BioNTech и Pfizer для детей в возрасте от пяти до одиннадцати лет! Об этом ЕМА объявило 18 октября в Амстердаме. Уже ранее наспех были одобрены спорные генные вакцины сначала для взрослых, а затем и для подростков с двенадцатилетнего возраста. EMA, которое отвечает за одобрение и мониторинг лекарственных средств в ЕС, выступает в качестве экспертного органа. Но насколько надёжным и, прежде всего, независимым является это агентство, учитывая тот факт, что "вакцина" скоро будет вводиться и самым маленьким? Эмер Кук была назначена директором ЕМА 16 ноября 2020 года. Ее мнение является решающим при одобрении фармацевтического продукта. Откуда она появилась? - С 1985 по 1991 год Эмер Кук работала на различных должностях в ирландской фармацевтической промышленности. - В 1991 году она вошла в состав правления Европейской федерации фармацевтической промышленности и ассоциаций (EFPIA). EFPIA является самой важной лоббистской организацией в фармацевтической промышленности, с наибольшими расходами на лоббирование, наибольшим количеством контактов с ЕС и несколькими лоббистскими агентствами. В ней представлены некоторые из мировых крупнейших фармацевтических компаний, включая AstraZeneca, Johnson & Johnson и Pfizer. До 1998 года Кук представляла интересы именно этих фармацевтических компаний в сфере регулирования. - С 1998 по 2002 год Эмер Кук возглавляла фармацевтический отдел ЕС-комиссии. Оттуда она перешла в ЕМА, где до 2016 года занимала должность руководителя инспекции и должность руководителя отдела международных отношений. - С ноября 2016 года по ноябрь 2020 года занимала должность исполнительного директора EMA и отвечала за всю регуляторную деятельность, связанную с фармацевтической продукцией. После того как Эмер Кук заняла пост в ЕМА, в течение очень короткого времени были одобрены вакцины против ковида для ЕС от следующих фармацевтических компаний: - 21 декабря 2020 года – от компаний Pfizer и BioNTech, - 29 января 2021 года - от AstraZeneca, - 12 марта 2021 года – от компании Johnson&Johnson. Когда стало известно о многочисленных случаях тромбоза вен головного мозга, в том числе со смертельным исходом, в связи с вакцинацией, проводимой компанией AstraZeneca, Эмер Кук, в частности, выступила в защиту разрешения со стороны ЕС. Кстати, общий бюджет EMA на 2021 год составляет 386 миллионов евро. Из них 330 миллионов евро приходится только на сборы за одобрение фармацевтических компаний, то есть около 86 процентов. Член парламента Австрии Геральд Хаузер задаётся вопросом, может ли человек с такими мощными корнями в фармацевтике, как Эмер Кук, беспристрастно принимать решения о выдаче лицензий на продажу: "Так, доктор Эмер Кук, которая была назначена членом правления EMA в середине ноября 2020 года, всю свою жизнь проработала в фармацевтической промышленности. Занимая руководящие должности, она лоббировала интересы фармацевтической промышленности и сейчас отвечает за утверждение, контроль и эффективность вакцин - в том числе и для компании AstraZeneca. Уважаемые коллеги. Что можно сказать, даже не будучи опытным парламентарием, в таком случае? Что можно сказать? Откровенная инсайдерская торговля, откровенное кумовство, взяточничество и всё возможное. Так оно и есть. Пожалуйста, подумайте об этом, когда будете ссылаться на ЕМА в качестве доказательства правильности тестирования медицинских препаратов". Поэтому совершенно естественно возникает вопрос о доверии к EMA: прививка, которая уже сейчас вызывает больше смертей и побочных эффектов, чем все остальные "вакцины", вместе взятые, должна защитить маленьких детей от болезни? Инъекция, которая приносит миллиарды фармацевтическим компаниям, должна быть полезной для детей?! Прибыль корпораций за 2020 год и 1 квартал 2021 года: Pfizer: 14 500 млн $, Johnson&Johnson: 21 600 млн $, BioNTech: 1 100 млн €.
от ag./ah.
Vermögenszuwachs der Milliardäre und Pharma: https://inequality.org/great-divide/10-biggest-pandemic-profiteers/
vom 23.3.2021 www,kla,tv/19606 : Обзор корона-обдираловки Emer Cookes Lobbytätigkeit https://de.rt.com/europa/115540-ema-direktorin-jahrelang-lobbyistin-pharmaindustrie/
www.ots.at/presseaussendung/OTS_20210401_OTS0032/fpoe-hauser-ema-direktorin-hat-ihr-ganzes-arbeitsleben-mit-lobbying-fuer-die-pharmaindustrie-verbracht
https://deutsche-wirtschafts-nachrichten.de/510959/EU-Direktorin-fuer-Impfstoff-Zulassung-war-Pharma-Lobbyistin-unter-anderem-fuer-AstraZeneca
https://lobbypedia.de/wiki/European_Federation_of_Pharmaceutical_Industries_and_Associations
www.ema.europa.eu/en/about-us/who-we-are/executive-director
Rede von Gerald Hauser: www.youtube.com/watch?v=oqH9CoXXYIs
www.kla.tv/18927:
Dringender Warnruf: EU-Kommission erteilt Impfzulassung für Kinder – wie vertrauenswürdig ist die Bewertung der EMA wirklich? EMA-Gebühren www.ema.europa.eu/en/human-regulatory/overview/fees-payable-european-medicines-agency
Todesfälle durch Impfung: Open VAERS, (2021) VAERS COVID vaccine data Open VAERS, (2021) All deaths reported to VAERS by year https://doctors4covidethics.org/as/
https://tkp.at/2021/09/16/offener-brief-von-aerzten-und-wissenschaftlern-an-ema-und-eu-parlament/