{"id":22695,"date":"2019-10-04T11:11:24","date_gmt":"2019-10-04T09:11:24","guid":{"rendered":"https:\/\/kymos.com\/news\/que-passa-amb-les-proves-per-lots-i-lalliberament-per-lots-despres-del-brexit\/"},"modified":"2019-10-04T11:11:24","modified_gmt":"2019-10-04T09:11:24","slug":"que-passa-amb-les-proves-per-lots-i-lalliberament-per-lots-despres-del-brexit","status":"publish","type":"post","link":"https:\/\/kymos.com\/ca\/news\/que-passa-amb-les-proves-per-lots-i-lalliberament-per-lots-despres-del-brexit\/","title":{"rendered":"Qu\u00e8 passa amb les proves per lots i l&#8217;alliberament per lots despr\u00e9s del Brexit?"},"content":{"rendered":"<p><span style=\"font-size: 14pt;\">Kymos compleix amb les inspeccions de la FDA i l&#8217;EMA, aix\u00ed com amb els est\u00e0ndards GLP, GMP i GCP. En particular, com a CRO certificada per GMP, assumim la responsabilitat de proporcionar l&#8217;autoritzaci\u00f3 del fabricant per a fins de control de qualitat. En aquesta guia, Kymos ajuda a descriure la situaci\u00f3 actual del Brexit i qu\u00e8 significa aix\u00f2 per a <a href=\"https:\/\/kymos.com\/ca\/serveis\/cmc-analisi-i-control-de-qualitat\/prova-de-lots-i-llancament-de-lots\/\" data-wpel-link=\"internal\">les proves de lots i l&#8217;alliberament de lots<\/a> despr\u00e9s del Brexit.    <\/span><\/p>\n<div class=\"blog-content\">\n<div class=\"field field-name-body field-type-text-with-summary field-label-hidden\">\n<div class=\"field-items\">\n<div class=\"field-item even\">\n<p><span style=\"font-size: 14pt;\">Actualment membre de l&#8217;EEE (Espai Econ\u00f2mic Europeu), el Regne Unit podria perdre els seus privilegis actuals a causa de la ruptura d&#8217;acords internacionals causats pel Brexit. Aquests acords s&#8217;hauran de negociar i aix\u00f2 podria afectar la fabricaci\u00f3 de medicaments. Actualment, el govern del Regne Unit est\u00e0 negociant amb la UE per minimitzar l&#8217;impacte del Brexit. Si les negociacions fracassen, la pres\u00e8ncia del Regne Unit com a membre de l&#8217;EMA (Ag\u00e8ncia Europea de Medicaments) podria deixar de ser possible. L&#8217;EMA ha traslladat la seva seu a Amsterdam com a conseq\u00fc\u00e8ncia de la retirada del Regne Unit de la UE.    <\/span><\/p>\n<p><span style=\"font-size: 14pt;\"><strong>Proves per lots i alliberament per lots despr\u00e9s de la data l\u00edmit del Brexit sense acord<\/strong><\/span><\/p>\n<p><span style=\"font-size: 14pt;\">Actualment, els acords de proves de lots i d&#8217;alliberament de lots funcionen de manera senzilla: els fabricants poden provar lots de medicaments de pa\u00efsos de la UE, l&#8217;EEE o tercers pa\u00efsos si estan coberts per un <a href=\"https:\/\/www.ema.europa.eu\/en\/human-regulatory-overview\/research-development\/compliance-research-development\/good-manufacturing-practice\/mutual-recognition-agreements-mra\" data-wpel-link=\"external\">Acord de Reconeixement Mutu<\/a> (MRA). A causa de la retirada de la UE, el Regne Unit es convertir\u00e0 en un &#8220;tercer pa\u00eds&#8221;, la qual cosa implica que &#8220;tot el dret primari i secundari de la Uni\u00f3 deixa d&#8217;aplicar-se al Regne Unit a partir del 30 de mar\u00e7 de 2019, a les 00:00 h (CET)&#8221;, segons <a href=\"https:\/\/www.gmp-compliance.org\/gmp-news\/brexit-u-k-will-become-third-country-according-to-eu-statement\" target=\"_blank\" rel=\"noopener\" data-wpel-link=\"external\">aquesta Declaraci\u00f3 de la UE<\/a> . <\/span><\/p>\n<p><span style=\"font-size: 14pt;\">Per minimitzar les interrupcions, el govern brit\u00e0nic ha estat treballant per complir els acords internacionals en cas d&#8217;un escenari sense acord. Per garantir la continu\u00eftat del subministrament de medicaments, la MHRA (Ag\u00e8ncia Reguladora de Medicaments i Productes Sanitaris) ha preparat una llista dels pa\u00efsos (inclosos la UE, l&#8217;EEE i tercers pa\u00efsos amb un MRA) que continuaran acceptant proves per lots. <\/span><br \/>\n<span style=\"font-size: 14pt;\">Una de les normes principals, segons l&#8217;article 51(1) de la Directiva 2001\/83\/CE i l&#8217;article 55(1) de la Directiva 2001\/82\/CE, estableix que tots els medicaments destinats al mercat de la UEE s&#8217;han de fabricar d&#8217;acord amb els requisits de bones pr\u00e0ctiques de fabricaci\u00f3 (BPM) de la Uni\u00f3 i l&#8217;autoritzaci\u00f3 de comercialitzaci\u00f3 (MA). Per tant, el lloc de llan\u00e7ament del lot ha d&#8217;estar ubicat en un dels pa\u00efsos de l&#8217;EEE. <\/span><br \/>\n<span style=\"font-size: 14pt;\">Aix\u00f2 significa que totes les empreses farmac\u00e8utiques del Regne Unit que vulguin comercialitzar els seus productes en un pa\u00eds de la UE han de trobar una seu registrada i amb llic\u00e8ncia de la UE\/EEE. Aix\u00f2 tamb\u00e9 s&#8217;aplica a altres activitats com l&#8217;alliberament de lots i les activitats de farmacovigil\u00e0ncia, que han de ser realitzades per una QP i una QPPV situades a la UE\/EEE. <\/span><\/p>\n<p><span style=\"font-size: 14pt;\">A Kymos, ens prenem molt seriosament l&#8217;alliberament i les proves de lots i ens comprometem a mantenir-vos informats. Si necessiteu m\u00e9s informaci\u00f3, poseu-vos en contacte amb nosaltres al +34 935 481 848, envieu un correu electr\u00f2nic a <a href=\"mailto:info@kymos.com\" data-wpel-link=\"internal\">info@kymos.com<\/a> o, si sou a Barcelona el 31 d&#8217;octubre, uniu-vos a nosaltres al seminari sobre els efectes del Brexit en el sector farmac\u00e8utic. <\/span><\/p>\n<p><span style=\"font-size: 14pt;\"><strong>Orientaci\u00f3 i informaci\u00f3 institucionals<\/strong><\/span><\/p>\n<p><span style=\"font-size: 14pt;\">El <a href=\"https:\/\/www.ema.europa.eu\/en\/homepage\" data-wpel-link=\"external\">lloc web de l&#8217;EMA<\/a> proporciona informaci\u00f3 per ajudar a preparar les companyies farmac\u00e8utiques de medicaments humans i veterinaris per a la situaci\u00f3 del Brexit al Regne Unit.<\/span><br \/>\n<span style=\"font-size: 14pt;\">Aquesta informaci\u00f3 cont\u00e9 els documents actualitzats seg\u00fcents:<\/span><\/p>\n<ul>\n<li><span style=\"font-size: 14pt;\"><a href=\"https:\/\/www.ema.europa.eu\/en\/documents\/regulatory-procedural-guideline\/practical-guidance-procedures-related-brexit-medicinal-products-human-and-veterinary-use-within-framework-centralised-procedure_en.pdf\" target=\"_blank\" rel=\"noopener\" data-wpel-link=\"external\">Guia pr\u00e0ctica de l&#8217;EMA<\/a><\/span><\/li>\n<li><span style=\"font-size: 14pt;\"><a href=\"https:\/\/www.ema.europa.eu\/en\/human-regulatory-overview\/post-authorisation\/data-medicines-iso-idmp-standards-post-authorisation\/reporting-requirements-marketing-authorisation-holders\" target=\"_blank\" rel=\"noopener\" data-wpel-link=\"external\">Comunicaci\u00f3 de la Comissi\u00f3 Europea\/EMA als titulars d&#8217;autoritzacions de comercialitzaci\u00f3<\/a><\/span><\/li>\n<li><a href=\"https:\/\/www.ema.europa.eu\/en\/documents\/regulatory-procedural-guideline\/notice-stakeholders-withdrawal-united-kingdom-and-eu-rules-medicinal-products-human-use-and-veterinary-medicinal-products_en.pdf\" target=\"_blank\" rel=\"noopener\" data-wpel-link=\"external\"><span style=\"font-size: 14pt;\">Retirada del Regne Unit i de les normes de la UE per a medicaments d&#8217;\u00fas hum\u00e0 i medicaments veterinaris<\/span><\/a><\/li>\n<\/ul>\n<p><span style=\"font-size: 14pt;\">Per tal de facilitar la transici\u00f3 entre la situaci\u00f3 antiga i la nova possible, el govern del Regne Unit tamb\u00e9 est\u00e0 publicant informaci\u00f3 a les empreses amb seu al Regne Unit per preparar-les per a l&#8217;escenari sense acord.<\/span><\/p>\n<ul>\n<li><span style=\"font-size: 14pt;\"><a href=\"https:\/\/www.gov.uk\/government\/publications\/batch-testing-medicines-if-theres-no-brexit-deal\/batch-testing-medicines-if-theres-no-brexit-deal\" target=\"_blank\" rel=\"noopener\" data-wpel-link=\"external\">Proves per lots de medicaments si no hi ha acord del Brexit<\/a><\/span><\/li>\n<li><span style=\"font-size: 14pt;\"><a href=\"https:\/\/www.gov.uk\/government\/publications\/submitting-regulatory-information-on-medical-products-if-theres-no-brexit-deal\/submitting-regulatory-information-on-medical-products-if-theres-no-brexit-deal\" target=\"_blank\" rel=\"noopener\" data-wpel-link=\"external\">Presentaci\u00f3 d&#8217;informaci\u00f3 reglament\u00e0ria sobre productes m\u00e8dics si no hi ha acord sobre el Brexit<\/a><\/span><\/li>\n<li><span style=\"font-size: 14pt;\"><a href=\"https:\/\/www.gov.uk\/government\/publications\/further-guidance-note-on-the-regulation-of-medicines-medical-devices-and-clinical-trials-if-theres-no-brexit-deal\/further-guidance-note-on-the-regulation-of-medicines-medical-devices-and-clinical-trials-if-theres-no-brexit-deal\" target=\"_blank\" rel=\"noopener\" data-wpel-link=\"external\">Nota d&#8217;orientaci\u00f3 addicional sobre la regulaci\u00f3 de medicaments, dispositius m\u00e8dics i assajos cl\u00ednics si no hi ha acord sobre el Brexit<\/a><\/span><\/li>\n<\/ul>\n<p><span style=\"font-size: 14pt;\">En el futur es podria publicar nova informaci\u00f3. Les darreres not\u00edcies suggereixen que la implementaci\u00f3 d&#8217;un acord del Brexit podria retardar-se i, per tant, la situaci\u00f3 pot canviar di\u00e0riament. <\/span><\/p>\n<p><span style=\"font-size: 14pt;\"><strong>Refer\u00e8ncies<\/strong><\/span><br \/>\n<span style=\"font-size: 14pt;\"><a href=\"https:\/\/www.ema.europa.eu\/en\/documents\/regulatory-procedural-guideline\/practical-guidance-procedures-related-brexit-medicinal-products-human-and-veterinary-use-within-framework-centralised-procedure_en.pdf\" target=\"_blank\" rel=\"noopener\" data-wpel-link=\"external\">Guia pr\u00e0ctica per als procediments relacionats amb el Brexit per a medicaments d&#8217;\u00fas hum\u00e0 i veterinari en el marc del procediment centralitzat [PDF]  <\/a><\/span><br \/>\n<span style=\"font-size: 14pt;\"><a href=\"https:\/\/www.gmp-compliance.org\/gmp-news\/brexit-u-k-will-become-third-country-according-to-eu-statement\" target=\"_blank\" rel=\"noopener\" data-wpel-link=\"external\">Brexit: el Regne Unit es convertir\u00e0 en un &#8220;tercer pa\u00eds&#8221;, segons un comunicat de la UE<\/a><\/span><br \/>\n<span style=\"font-size: 14pt;\"><a href=\"https:\/\/www.telegraph.co.uk\/politics\/2019\/03\/02\/brexit-delay-now-unavoidable-says-eu-andrea-leadsom-jeremy-hunt\/\" target=\"_blank\" rel=\"noopener\" data-wpel-link=\"external\">La UE afirma que l&#8217;ajornament del Brexit ara \u00e9s inevitable, mentre Andrea Leadsom i Jeremy Hunt alerten d&#8217;un intent de frustrar la sortida  <\/a><\/span><\/p>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n","protected":false},"excerpt":{"rendered":"<p>Kymos compleix amb les inspeccions de la FDA i l&#8217;EMA,  [&#8230;]<\/p>\n","protected":false},"author":6,"featured_media":14973,"comment_status":"","ping_status":"","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[97,106],"tags":[],"class_list":["post-22695","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-cmc-ca","category-novetats"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.3 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Proves per lots i alliberament de lots despr\u00e9s del Brexit | Kymos Group<\/title>\n<meta name=\"description\" content=\"M\u00e9s informaci\u00f3 sobre com Kymos ajuda a definir la situaci\u00f3 actual del Brexit i qu\u00e8 significa aix\u00f2 per a les proves per lots i l&#039;alliberament de lots despr\u00e9s del Brexit.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link 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Dou\",\"image\":{\"@type\":\"ImageObject\",\"inLanguage\":\"ca\",\"@id\":\"https:\\\/\\\/secure.gravatar.com\\\/avatar\\\/263d7ff1c7891f5821a5075a1a362a1e513db5931dc882455e887fe1c1ccf924?s=96&d=mm&r=g\",\"url\":\"https:\\\/\\\/secure.gravatar.com\\\/avatar\\\/263d7ff1c7891f5821a5075a1a362a1e513db5931dc882455e887fe1c1ccf924?s=96&d=mm&r=g\",\"contentUrl\":\"https:\\\/\\\/secure.gravatar.com\\\/avatar\\\/263d7ff1c7891f5821a5075a1a362a1e513db5931dc882455e887fe1c1ccf924?s=96&d=mm&r=g\",\"caption\":\"Joan Puig de Dou\"},\"description\":\"Active in the pharmaceutical marketing for over 30 years President of CataloniaBIO&amp;HealthTech CEO and Qualified Person at Kymos Leader of Kymos team, guaranteeing a trustable, ethical and scientific correct editorial publications. Experience Joan Puig de Dou started his career at Laboratorios Menarini first as scientist later as Qualified Person and finally as Operations General Manager. 2010 he entered Kymos where he became CEO in 2015. 2022 Joan Puig de Dou was elected as president of CataloniaBio&amp;HealthTech to represent the Catalonian biotech industry nationally and internationally. Expertise Joan Puig de Dou has extensive experience in writing scientific content adopting a didactic approach that fits any reader\u2019s level of expertise. He publishes regularely on Kymos\u2019 webpage, social media and in the specialized press. Education He graduated from Universitat de Barcelona as Pharmacist and from IESE Business School\u2019s Programa Diecci\u00f3n General (PDG) Want to know him better? 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Dou","image":{"@type":"ImageObject","inLanguage":"ca","@id":"https:\/\/secure.gravatar.com\/avatar\/263d7ff1c7891f5821a5075a1a362a1e513db5931dc882455e887fe1c1ccf924?s=96&d=mm&r=g","url":"https:\/\/secure.gravatar.com\/avatar\/263d7ff1c7891f5821a5075a1a362a1e513db5931dc882455e887fe1c1ccf924?s=96&d=mm&r=g","contentUrl":"https:\/\/secure.gravatar.com\/avatar\/263d7ff1c7891f5821a5075a1a362a1e513db5931dc882455e887fe1c1ccf924?s=96&d=mm&r=g","caption":"Joan Puig de Dou"},"description":"Active in the pharmaceutical marketing for over 30 years President of CataloniaBIO&amp;HealthTech CEO and Qualified Person at Kymos Leader of Kymos team, guaranteeing a trustable, ethical and scientific correct editorial publications. Experience Joan Puig de Dou started his career at Laboratorios Menarini first as scientist later as Qualified Person and finally as Operations General Manager. 2010 he entered Kymos where he became CEO in 2015. 2022 Joan Puig de Dou was elected as president of CataloniaBio&amp;HealthTech to represent the Catalonian biotech industry nationally and internationally. Expertise Joan Puig de Dou has extensive experience in writing scientific content adopting a didactic approach that fits any reader\u2019s level of expertise. He publishes regularely on Kymos\u2019 webpage, social media and in the specialized press. Education He graduated from Universitat de Barcelona as Pharmacist and from IESE Business School\u2019s Programa Diecci\u00f3n General (PDG) Want to know him better? Read his interview in PharmaBoardrooom in January 2019 and more about his presidency of CataloniaBio at Parc Sc\u00edentific de Barcelona.","url":"https:\/\/kymos.com\/ca\/news\/author\/joan-puig-de-dou\/"}]}},"_links":{"self":[{"href":"https:\/\/kymos.com\/ca\/wp-json\/wp\/v2\/posts\/22695","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/kymos.com\/ca\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/kymos.com\/ca\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/kymos.com\/ca\/wp-json\/wp\/v2\/users\/6"}],"replies":[{"embeddable":true,"href":"https:\/\/kymos.com\/ca\/wp-json\/wp\/v2\/comments?post=22695"}],"version-history":[{"count":0,"href":"https:\/\/kymos.com\/ca\/wp-json\/wp\/v2\/posts\/22695\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/kymos.com\/ca\/wp-json\/wp\/v2\/media\/14973"}],"wp:attachment":[{"href":"https:\/\/kymos.com\/ca\/wp-json\/wp\/v2\/media?parent=22695"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/kymos.com\/ca\/wp-json\/wp\/v2\/categories?post=22695"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/kymos.com\/ca\/wp-json\/wp\/v2\/tags?post=22695"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}