{"id":8826,"date":"2020-05-10T14:20:12","date_gmt":"2020-05-10T06:20:12","guid":{"rendered":"https:\/\/www.sqi.org.sg\/?post_type=lp_course&#038;p=8826"},"modified":"2026-01-09T00:28:50","modified_gmt":"2026-01-08T16:28:50","slug":"iso-134852016-medical-devices-ia-training","status":"publish","type":"lp_course","link":"https:\/\/www.staging.sqi.org.sg\/staging\/courses\/iso-134852016-medical-devices-ia-training\/","title":{"rendered":"ISO 13485:2016 MEDICAL DEVICES &#038; IA TRAINING"},"content":{"rendered":"<h4>Objectives<\/h4>\n<p>ISO 13485:2016 specifies requirements for a quality management system where an organisation needs to demonstrate its ability to provide medical devices and related services that consistently meet customer and applicable regulatory requirements.<\/p>\n<ul>\n<li>The functions &amp; requirements of the ISO 13485:2016 Medical Devices standard.<\/li>\n<li>The understanding &amp; implementing of the ISO 13485 Medical Devices standard effectively as to work instructions \/ standard operation procedure manuals requirements.<\/li>\n<li>Using ISO 13485 Medical Devices standard to drive towards becoming a quality class organisation.<\/li>\n<\/ul>\n<h4>Duration<\/h4>\n<p>2 days | 9am \u2013 5pm | 14 hours<\/p>\n<h4>Who should attend<\/h4>\n<p style=\"text-align: justify;\">Managers, executives, supervisors and management staff who want to gain knowledge on ISO 13485:2016 Medical Devices and staff who are likely or currently involved in implementing and maintaining ISO 13485:2003 and key personnel assigned for internal audits, management representatives (MR), etc.<\/p>\n<h4>Key Benefits<\/h4>\n<p>A trained-combined system Internal Auditor with the skill set to:<\/p>\n<ul>\n<li>Conduct an internal audit of the ISO 13485 management system.<\/li>\n<li>Enable your business to remain compliant with the requirements of the ISO 134845.<\/li>\n<li>Follow through complex audit trails and identify any possible management systems discrepancies.<\/li>\n<li>Identify any gaps that threaten the effectiveness of your management systems.<\/li>\n<\/ul>\n<h4>Course Fees<\/h4>\n<p data-pm-slice=\"1 1 []\">Member Fee: S $782.62<br \/>\nNon-Member Fee: S $867.64 <\/p>\n<p><small><small><em>All fees stated are inclusive of Registration Fee and 9% GST.<\/em><\/small><\/small><\/p>\n<h4>Award of Certificate<\/h4>\n<p>Certificate of Completion will be issued to participants who have attended at least 75% of the course.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Objectives ISO 13485:2016 specifies requirements for a quality management system where an organisation needs to demonstrate its ability to provide medical devices and related services that consistently meet customer and applicable regulatory requirements. The functions &amp; requirements of the ISO 13485:2016 Medical Devices standard. The understanding &amp; implementing of the ISO 13485 Medical Devices standard&#8230;<\/p>\n","protected":false},"author":1,"featured_media":14526,"comment_status":"open","ping_status":"closed","template":"","course_category":[69],"course_tag":[76],"class_list":["post-8826","lp_course","type-lp_course","status-publish","has-post-thumbnail","hentry","course_category-iso-standards","course_tag-iso_standards","pmpro-has-access","course"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.3 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>ISO 13485:2016 MEDICAL DEVICES &amp; IA TRAINING - Singapore Quality Institute<\/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.staging.sqi.org.sg\/staging\/courses\/iso-134852016-medical-devices-ia-training\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"ISO 13485:2016 MEDICAL DEVICES &amp; IA TRAINING - Singapore Quality Institute\" \/>\n<meta property=\"og:description\" content=\"Objectives ISO 13485:2016 specifies requirements for a quality management system where an organisation needs to demonstrate its ability to provide medical devices and related services that consistently meet customer and applicable regulatory requirements. The functions &amp; requirements of the ISO 13485:2016 Medical Devices standard. 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