{"id":2420,"date":"2021-07-16T19:28:20","date_gmt":"2021-07-16T19:28:20","guid":{"rendered":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/?post_type=policy-training&p=2420"},"modified":"2025-02-06T12:05:28","modified_gmt":"2025-02-06T12:05:28","slug":"engagement-with-external-stakeholders-session-may-18-2021-who","status":"publish","type":"policy-training","link":"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/training-and-capacity-building-resources\/policy-training\/engagement-with-external-stakeholders-session-may-18-2021-who\/","title":{"rendered":"Engagement with External Stakeholders Session \u2013 May 18, 2021 \u2013 WHO"},"content":{"rendered":"\n

WHO Relevant Recent Publications on Good Regulatory Practices, Good Reliance Practices and Post-market Surveillance were introduced by the leaders responsible for their development at the WHO, with the purpose to get the Coalition\u2019s members becoming familiar with them and promote a wider utilization.<\/p>\n\n\n\n

Presentation on Good regulatory practices for regulatory oversight of medical products and Good reliance practices in regulatory decision-making: high-level principles and recommendations by Marie Valentin is available in English<\/a>.<\/p>\n\n\n\n

Presentation on Guidance for post-market surveillance and market surveillance of medical devices, including in vitro diagnostics by Leticia Megias \/Anita Sands is available in English<\/a>.<\/p>\n\n\n\n

Links to the documents in English and to non-official translations to Portuguese and Spanish are available as follows:<\/p>\n\n\n\n

Presentations<\/h2>\n\n\n\n
WHO Good Regulatory Practices and Good Reliance Practices – Marie Valentin – WHO – Global<\/strong><\/h5>\n\n\n\n
Good Regulatory Practices<\/h5>\n\n\n\n
\n
English<\/a><\/div>\n\n\n\n
Spanish<\/a><\/div>\n\n\n\n
Portuguese<\/a><\/div>\n<\/div>\n\n\n\n
Good Reliance Practices<\/h5>\n\n\n\n
\n
English<\/a><\/div>\n\n\n\n
Spanish<\/a><\/div>\n\n\n\n
Portuguese<\/a><\/div>\n<\/div>\n\n\n\n
WHO guidance on post-market and market surveillance of medical devices including IVDs – Leticia Megias Lastra – WHO – Global<\/strong><\/h5>\n\n\n\n
\n
English<\/a><\/div>\n\n\n\n
Spanish<\/a><\/div>\n\n\n\n
Portuguese<\/a><\/div>\n<\/div>\n","protected":false},"parent":0,"menu_order":0,"template":"","event_category":[],"class_list":["post-2420","policy-training","type-policy-training","status-publish","hentry","description-off"],"acf":[],"yoast_head":"\nEngagement with External Stakeholders Session \u2013 May 18, 2021 \u2013 WHO - Regulatory Convergence<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.interamericancoalition-medtech.org\/regulatory-convergence\/training-and-capacity-building-resources\/policy-training\/engagement-with-external-stakeholders-session-may-18-2021-who\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Engagement with External Stakeholders Session \u2013 May 18, 2021 \u2013 WHO - Regulatory Convergence\" \/>\n<meta property=\"og:description\" content=\"WHO Relevant Recent Publications on Good Regulatory Practices, Good Reliance Practices and Post-market Surveillance were introduced by the leaders responsible for their development at the WHO, with the purpose to get the Coalition\u2019s members becoming familiar with them and promote a wider utilization. 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