{"id":4587,"date":"2023-06-12T21:55:01","date_gmt":"2023-06-12T21:55:01","guid":{"rendered":"https:\/\/staging.interamericancoalition-medtech.org\/regulatory-convergence\/?post_type=regulator-sessions&#038;p=4587"},"modified":"2024-01-18T12:13:40","modified_gmt":"2024-01-18T12:13:40","slug":"stability-medical-devices-webinar","status":"publish","type":"policy-training","link":"https:\/\/staging.interamericancoalition-medtech.org\/regulatory-convergence\/training-and-capacity-building-resources\/policy-training\/stability-medical-devices-webinar\/","title":{"rendered":"Stability \u2013 Medical Devices Webinar"},"content":{"rendered":"\n<p class=\"justified\">The Medical Device Regulatory Convergence Project, co-led by USAID, ANSI, and AdvaMed through the Inter-American Coalition for Regulatory Convergence in the Medical Technology Sector, in collaboration with the U.S. Food and Drug Administration (FDA), hosted a webinar on June 1 to present <strong>\u201cFundamentals of establishing sterile barrier systems for medical devices: package stability (shelf life) and package performance\u201d<\/strong> the <strong>\u201cConsiderations for assessing use-life of reusable devices\u201d<\/strong>, presented by Steven Turtil and the \u201cAssessing device performance for the labelled shelf-life\u201d, presented by Limin Sun.<\/p>\n\n\n\n<p class=\"justified mb-3\">The agenda, presentations and recorded session are available below.<\/p>\n\n\n\n<h2 class=\"wp-block-heading mb-0 has-accent-color has-text-color has-medium-font-size\">Agenda<\/h2>\n\n\n\n<div class=\"wp-block-buttons mb-3 is-layout-flex wp-block-buttons-is-layout-flex\">\n<div class=\"wp-block-button\"><a class=\"wp-block-button__link has-accent-background-color has-background wp-element-button\" href=\"https:\/\/staging.interamericancoalition-medtech.org\/regulatory-convergence\/wp-content\/uploads\/sites\/4\/2023\/06\/Webinar-Agenda-Stability-and-shelflife-of-medical-devices-1Jun23.pdf\" target=\"_blank\" rel=\"noreferrer noopener\">English<\/a><\/div>\n\n\n\n<div class=\"wp-block-button\"><a class=\"wp-block-button__link has-accent-background-color has-background wp-element-button\" href=\"https:\/\/staging.interamericancoalition-medtech.org\/regulatory-convergence\/wp-content\/uploads\/sites\/4\/2023\/06\/Webinar-Agenda-Stability-and-shelflife-of-medical-devices-1Jun23-Spanish.pdf\" target=\"_blank\" rel=\"noreferrer noopener\">Spanish<\/a><\/div>\n<\/div>\n\n\n\n<h2 class=\"wp-block-heading mb-0 has-accent-color has-text-color has-medium-font-size\">Recordings<\/h2>\n\n\n\n<div class=\"wp-block-buttons mb-3 is-layout-flex wp-block-buttons-is-layout-flex\">\n<div class=\"wp-block-button\"><a class=\"wp-block-button__link has-accent-background-color has-background wp-element-button\" href=\"https:\/\/youtu.be\/BUqY53fst_8\" target=\"_blank\" rel=\"noreferrer noopener\">English<\/a><\/div>\n\n\n\n<div class=\"wp-block-button\"><a class=\"wp-block-button__link has-accent-background-color has-background wp-element-button\" href=\"https:\/\/youtu.be\/4CgV15aL3eE\" target=\"_blank\" rel=\"noreferrer noopener\">Spanish<\/a><\/div>\n\n\n\n<div class=\"wp-block-button\"><a class=\"wp-block-button__link has-accent-background-color has-background wp-element-button\" href=\"https:\/\/youtu.be\/uQ4viqrU5fU\" target=\"_blank\" rel=\"noreferrer noopener\">Portuguese<\/a><\/div>\n<\/div>\n\n\n\n<h2 class=\"wp-block-heading mb-0 has-accent-color has-text-color has-medium-font-size\">Presentations<\/h2>\n\n\n\n<h5 class=\"wp-block-heading mb-1\" style=\"font-size:16px\"><strong>MEDICAL DEVICE STABILITY &#8211; Conducting Package Stability and Performance Validation for Terminally Sterilized Single-Use Medical Devices \u2014 and \u2014 Establishing Use-Life for Reusable Medical Devices &#8211; Steven Turtil , US FDA<\/strong><\/h5>\n\n\n\n<div class=\"wp-block-buttons mb-3 is-layout-flex wp-block-buttons-is-layout-flex\">\n<div class=\"wp-block-button\"><a class=\"wp-block-button__link has-accent-background-color has-background wp-element-button\" href=\"https:\/\/staging.interamericancoalition-medtech.org\/regulatory-convergence\/wp-content\/uploads\/sites\/4\/2023\/06\/STABILITY-PACKAGING-ANDREUSABLES-final-1.pdf\" target=\"_blank\" rel=\"noreferrer noopener\">English<\/a><\/div>\n\n\n\n<div class=\"wp-block-button\"><a class=\"wp-block-button__link has-accent-background-color has-background wp-element-button\" href=\"https:\/\/staging.interamericancoalition-medtech.org\/regulatory-convergence\/wp-content\/uploads\/sites\/4\/2023\/06\/STABILITY-PACKAGING-and-REUSABLES-Final-SP-1.pdf\" target=\"_blank\" rel=\"noreferrer noopener\">Spanish<\/a><\/div>\n<\/div>\n\n\n\n<h5 class=\"wp-block-heading mb-1\" style=\"font-size:16px\"><strong>Assessing device performance for the labelled shelf-life &#8211; Limin Sun, US FDA<\/strong><\/h5>\n\n\n\n<div class=\"wp-block-buttons mb-3 is-layout-flex wp-block-buttons-is-layout-flex\">\n<div class=\"wp-block-button\"><a class=\"wp-block-button__link has-accent-background-color has-background wp-element-button\" href=\"https:\/\/staging.interamericancoalition-medtech.org\/regulatory-convergence\/wp-content\/uploads\/sites\/4\/2023\/06\/product-shelf-life-presentation.Limin-Sun.Final_-1.pdf\" target=\"_blank\" rel=\"noreferrer noopener\">English<\/a><\/div>\n\n\n\n<div class=\"wp-block-button\"><a class=\"wp-block-button__link has-accent-background-color has-background wp-element-button\" href=\"https:\/\/staging.interamericancoalition-medtech.org\/regulatory-convergence\/wp-content\/uploads\/sites\/4\/2023\/06\/product-shelf-life-presentation.Limin-Sun-Final-SP-1.pdf\" target=\"_blank\" rel=\"noreferrer noopener\">Spanish<\/a><\/div>\n<\/div>\n","protected":false},"parent":0,"menu_order":0,"template":"","event_category":[],"class_list":["post-4587","policy-training","type-policy-training","status-publish","hentry","description-off"],"acf":[],"yoast_head":"<!-- This site is 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