{"id":3031,"date":"2023-04-25T07:06:01","date_gmt":"2023-04-25T07:06:01","guid":{"rendered":"https:\/\/conimcert.com\/?post_type=training&#038;p=3031"},"modified":"2023-05-16T17:52:18","modified_gmt":"2023-05-16T17:52:18","slug":"iso-13485-medical-devices-quality-ms-introduction","status":"publish","type":"training","link":"https:\/\/conimcert.com\/az\/training\/iso-13485-medical-devices-quality-ms-introduction\/","title":{"rendered":"ISO 13485 Tibbi Cihazlar\u0131n Keyfiyy\u0259t \u0130dar\u0259etm\u0259 Sisteml\u0259ri - Giri\u015f"},"content":{"rendered":"<p><strong>1. Q\u0131sa t\u0259svir:<\/strong><\/p>\n\n\n\n<p>ISO 13485 Tibbi Cihazlar\u0131n Keyfiyy\u0259t \u0130dar\u0259etm\u0259 Sistemi (K\u0130S) Giri\u015f sxemi i\u015ftirak\u00e7\u0131lara ISO 13485 standart\u0131na \u0259saslanan K\u0130S-in \u0259sas prinsipl\u0259ri v\u0259 t\u0259l\u0259bl\u0259ri haqq\u0131nda anlay\u0131\u015f verm\u0259k \u00fc\u00e7\u00fcn n\u0259z\u0259rd\u0259 tutulmu\u015fdur. Bu sxem tibbi cihazlar s\u0259nayesind\u0259 keyfiyy\u0259tin idar\u0259 edilm\u0259si haqq\u0131nda \u00f6yr\u0259nm\u0259kd\u0259 maraql\u0131 olan \u015f\u0259xsl\u0259r \u00fc\u00e7\u00fcn uy\u011fun olan giri\u015f s\u0259viyy\u0259li kursdur.<\/p>\n\n\n\n<p><strong>2. \u018fsas M\u00f6vzular:<\/strong><\/p>\n\n\n\n<p>ISO 13485 K\u0130S Giri\u015f t\u0259limind\u0259 \u0259hat\u0259 olunan \u0259sas m\u00f6vzulara a\u015fa\u011f\u0131dak\u0131lar daxildir:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Tibbi cihazlar s\u0259nayesind\u0259 keyfiyy\u0259tin idar\u0259 edilm\u0259sin\u0259 giri\u015f<\/li>\n\n\n\n<li>Keyfiyy\u0259tin idar\u0259 edilm\u0259sinin prinsip v\u0259 konsepsiyalar\u0131n\u0131 ba\u015fa d\u00fc\u015fm\u0259k<\/li>\n\n\n\n<li>K\u0130S \u00fc\u00e7\u00fcn ISO 13485 standart\u0131n\u0131n t\u0259l\u0259bl\u0259ri<\/li>\n\n\n\n<li>ISO 13485 standart\u0131na \u0259saslanan K\u0130S-nin t\u0259tbiqi<\/li>\n\n\n\n<li>K\u0130S-in davaml\u0131 t\u0259kmill\u0259\u015fdirilm\u0259si<\/li>\n<\/ul>\n\n\n\n<p><strong>3. Auditoriya:<\/strong><\/p>\n\n\n\n<p>ISO 13485 K\u0130S Giri\u015f t\u0259limi a\u015fa\u011f\u0131dak\u0131lar \u00fc\u00e7\u00fcn n\u0259z\u0259rd\u0259 tutulub:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Tibbi cihazlar s\u0259nayesind\u0259 keyfiyy\u0259tin idar\u0259 edilm\u0259si v\u0259 ISO 13485 standart\u0131 haqq\u0131nda t\u0259m\u0259l anlay\u0131\u015f \u0259ld\u0259 etm\u0259k ist\u0259y\u0259n \u015f\u0259xsl\u0259r<\/li>\n\n\n\n<li>Tibbi cihazlar \u00fc\u00e7\u00fcn K\u0130S-nin t\u0259tbiqi il\u0259 m\u0259\u015f\u011ful olan \u015f\u0259xsl\u0259r<\/li>\n\n\n\n<li>Tibbi cihazlar \u00fc\u00e7\u00fcn K\u0130S-in t\u0259tbiqi il\u0259 m\u0259\u015f\u011ful olan \u015f\u0259xsl\u0259r<\/li>\n<\/ul>\n\n\n\n<p><strong>4. T\u0259limin m\u0259qs\u0259dl\u0259ri:<\/strong><\/p>\n\n\n\n<p>ISO 13485 K\u0130S Giri\u015f kursunun sonunda i\u015ftirak\u00e7\u0131lar a\u015fa\u011f\u0131dak\u0131lar\u0131 ed\u0259 bil\u0259c\u0259kl\u0259r:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Tibbi cihazlar s\u0259nayesind\u0259 keyfiyy\u0259tin idar\u0259 edilm\u0259sinin \u0259sas anlay\u0131\u015flar\u0131n\u0131 v\u0259 prinsipl\u0259rini anlayacaq<\/li>\n\n\n\n<li>K\u0130S \u00fc\u00e7\u00fcn ISO 13485 standart\u0131n\u0131n m\u0259qs\u0259dini v\u0259 t\u0259l\u0259bl\u0259rini izah ed\u0259c\u0259k<\/li>\n\n\n\n<li>K\u0130S-nin \u0259sas komponentl\u0259rini v\u0259 onlar\u0131n nec\u0259 h\u0259yata ke\u00e7iril\u0259 bil\u0259c\u0259yini m\u00fc\u0259yy\u0259nl\u0259\u015fdir\u0259c\u0259k<\/li>\n\n\n\n<li>ISO 13485 standart\u0131na \u0259saslanan K\u0130S t\u0259tbiqinin faydalar\u0131n\u0131 t\u0259svir ed\u0259c\u0259k<\/li>\n\n\n\n<li>Tibbi cihazlar \u00fc\u00e7\u00fcn K\u0130S-nin davaml\u0131 t\u0259kmill\u0259\u015fdirilm\u0259sinin vacibliyini d\u0259rk ed\u0259c\u0259k.<\/li>\n<\/ul>","protected":false},"featured_media":1549,"parent":0,"menu_order":0,"template":"","cert_category":[64],"discipline":[78,73,103,70],"class_list":["post-3031","training","type-training","status-publish","has-post-thumbnail","hentry","cert_category-iso","discipline-asset-management","discipline-occupational-health-and-safety-management","discipline-lean-management","discipline-quality-management-system"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v20.5 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>ISO 13485 Medical Devices Quality MS - Introduction - Conimcert<\/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:\/\/conimcert.com\/az\/training\/iso-13485-medical-devices-quality-ms-introduction\/\" \/>\n<meta property=\"og:locale\" content=\"az_AZ\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"ISO 13485 Medical Devices Quality MS - Introduction - Conimcert\" \/>\n<meta property=\"og:description\" content=\"1. 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