{"id":38988,"date":"2020-07-28T03:00:56","date_gmt":"2020-07-28T10:00:56","guid":{"rendered":"https:\/\/www.jamasoftware.com\/?p=38988"},"modified":"2023-01-12T16:50:26","modified_gmt":"2023-01-13T00:50:26","slug":"move-from-document-based-design-control-and-risk-management","status":"publish","type":"post","link":"https:\/\/www.jamasoftware.com\/legacy\/blog\/2020\/07\/28\/move-from-document-based-design-control-and-risk-management\/","title":{"rendered":"Medical Device Webinar: Move from Document-Based Design Control and Risk Management"},"content":{"rendered":"<p><img decoding=\"async\" class=\"aligncenter size-full wp-image-39074\" src=\"https:\/\/www.jamasoftware.com\/media\/2020\/07\/2020-08_Move-from-Document-Based-Design-Control-and-Risk-Management_Social-Image-1-1.png\" alt=\"\" width=\"1024\" height=\"512\" \/>Medical device companies are on the cutting-edge of advancing health care. Along with facing relentless pressures to innovate and release quality products, they also must comply with regulations and standards to remain competitive.<\/p>\n<p>On Tuesday, August 4th, we&#8217;ll be hosting a webinar specifically designed for product and<a href=\"https:\/\/www.jamasoftware.com\/solutions\/medical-device\/\"> engineering teams building medical devices<\/a>. We&#8217;ll be covering how to move beyond the frustrations of disconnected, document-based requirement systems, streamlining your design and development and risk management processes while maintaining compliance with applicable regulations and standards.<\/p>\n<hr \/>\n<h5><strong>Date:\u202f\u202f\u202f\u202f\u202f\u202f\u202f<\/strong> Tuesday, August 4th, 2020<br \/>\n<strong>Time:\u202f\u202f\u202f<\/strong>\u202f\u202f\u202f\u202f 8:00 &#8211; 9:00am PST<\/h5>\n<hr \/>\n<p>In this webinar, we&#8217;ll examine how <a href=\"https:\/\/resources.jamasoftware.com\/medical-device\/jama-connect-solution-for-medical-device-development\">Jama Connect for Medical Device Development<\/a> helps free your teams from document-based requirements management, streamline your processes, and spend more time on innovation. Register now to learn more about:<\/p>\n<ul class=\"fancy-list\">\n<li>Bringing systems thinking into design control and risk management activities using Jama Connect for Medical Device Development<\/li>\n<li>Aligning how you work with the development of the artifacts needed for compliance, the Design History File (DHF) and the Risk Management file (RMF)<\/li>\n<li>Defining products and risk controls through the lens of tracing<\/li>\n<li>Using Jama Connect to align your design control and risk management processes with relevant parts of governing regulations and standards ISO 13485:2016, 21 CFR 820.30, and ISO 14971:2018<\/li>\n<\/ul>\n<h5><\/h5>\n<h5>Presented by:<\/h5>\n<div class=\"row p-0\">\n<div class=\"col-3\"><img decoding=\"async\" class=\"aligncenter wp-image-38993\" src=\"https:\/\/www.jamasoftware.com\/media\/2020\/07\/zeb-geary-blue-150X150.png\" alt=\"\" width=\"150\" height=\"150\" \/><\/div>\n<div class=\"col-9\">\n<p><span data-contrast=\"none\"><b>Zeb Geary <\/b>&#8211; <\/span><span data-contrast=\"none\"><strong>Principal Cons<\/strong><\/span><b><span data-contrast=\"none\"><strong>u<\/strong>ltant, Jama Software<\/span><\/b><\/p>\n<p><span lang=\"EN-US\" xml:lang=\"EN-US\" data-contrast=\"auto\">Zeb brings<\/span><span lang=\"EN-US\" xml:lang=\"EN-US\" data-contrast=\"auto\">\u00a0more than 10 years\u202fof\u202fexperience in software consulting and business analysis<\/span><span lang=\"EN-US\" xml:lang=\"EN-US\" data-contrast=\"auto\">\u00a0to<\/span><span lang=\"EN-US\" xml:lang=\"EN-US\" data-contrast=\"auto\">\u00a0Jama\u2019s enterprise customers\u00a0<\/span><span lang=\"EN-US\" xml:lang=\"EN-US\" data-contrast=\"auto\">and\u00a0<\/span><span lang=\"EN-US\" xml:lang=\"EN-US\" data-contrast=\"auto\">help<\/span><span lang=\"EN-US\" xml:lang=\"EN-US\" data-contrast=\"auto\">s<\/span><span lang=\"EN-US\" xml:lang=\"EN-US\" data-contrast=\"auto\">\u00a0them deploy and optimize their use of\u00a0<\/span><span lang=\"EN-US\" xml:lang=\"EN-US\" data-contrast=\"auto\">the platform<\/span><span lang=\"EN-US\" xml:lang=\"EN-US\" data-contrast=\"auto\">. Over the past 3.5 years,\u00a0<\/span><span lang=\"EN-US\" xml:lang=\"EN-US\" data-contrast=\"auto\">he\u2019s<\/span><span lang=\"EN-US\" xml:lang=\"EN-US\" data-contrast=\"auto\">\u00a0worked closely with many regulated customers, especially within the Medical Device industry, to provide best practices and deployment assistance\u00a0<\/span><span lang=\"EN-US\" xml:lang=\"EN-US\" data-contrast=\"auto\">to better align<\/span><span lang=\"EN-US\" xml:lang=\"EN-US\" data-contrast=\"auto\">\u00a0<\/span><span lang=\"EN-US\" xml:lang=\"EN-US\" data-contrast=\"auto\">Jama<\/span><span lang=\"EN-US\" xml:lang=\"EN-US\" data-contrast=\"auto\">\u00a0Connect to regulated activities pertaining to design control and verification.<\/span><span lang=\"EN-US\" xml:lang=\"EN-US\" data-contrast=\"auto\">\u202f<\/span><\/p>\n<\/div>\n<\/div>\n<h5><\/h5>\n<h5 style=\"text-align: center;\">Watch the recording now!<\/h5>\n<p style=\"text-align: center;\"><a style=\"background-color: #d5502a; border-radius: 30px; color: #ffffff; display: inline-block; font-family: sans-serif; font-size: 13px; font-weight: bold; line-height: 40px; text-align: center; text-decoration: none; width: 200px; -webkit-text-size-adjust: none;\" href=\"https:\/\/go.jamasoftware.com\/move-from-document-based-design-control-and-risk-management-registration.html?utm_campaign=cta+blog\">WATCH NOW<\/a><\/p>\n<input class=\"fooboxshare_post_id\" type=\"hidden\" value=\"38988\"\/>","protected":false},"excerpt":{"rendered":"<p>Improve collaboration, quality, and delivery in medical device development by freeing your teams from document-based design control and risk management.<\/p>\n","protected":false},"author":4,"featured_media":47007,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"inline_featured_image":false,"footnotes":""},"categories":[4],"tags":[40,41,195],"industry":[574],"class_list":["post-38988","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-company-news","tag-medical-device-compliance","tag-medical-device-development","tag-webinar","industry-medical-devices"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO Premium plugin v28.1 (Yoast SEO v28.1) - 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