{"version":"1.0","provider_name":"OTAVA","provider_url":"https:\/\/www.otava.com","title":"FDA Regulation of Mobile Health Devices","type":"rich","width":600,"height":338,"html":"<blockquote class=\"wp-embedded-content\" data-secret=\"fHoTULyfbi\"><a href=\"https:\/\/www.otava.com\/blog\/fda-regulation-of-mobile-health-devices\/\">FDA Regulation of Mobile Health Devices<\/a><\/blockquote><iframe sandbox=\"allow-scripts\" security=\"restricted\" src=\"https:\/\/www.otava.com\/blog\/fda-regulation-of-mobile-health-devices\/embed\/#?secret=fHoTULyfbi\" width=\"600\" height=\"338\" title=\"&#8220;FDA Regulation of Mobile Health Devices&#8221; &#8212; OTAVA\" data-secret=\"fHoTULyfbi\" frameborder=\"0\" marginwidth=\"0\" marginheight=\"0\" scrolling=\"no\" class=\"wp-embedded-content\"><\/iframe><script type=\"text\/javascript\">\n\/* <![CDATA[ *\/\n\/*! This file is auto-generated *\/\n!function(d,l){\"use strict\";l.querySelector&&d.addEventListener&&\"undefined\"!=typeof URL&&(d.wp=d.wp||{},d.wp.receiveEmbedMessage||(d.wp.receiveEmbedMessage=function(e){var t=e.data;if((t||t.secret||t.message||t.value)&&!\/[^a-zA-Z0-9]\/.test(t.secret)){for(var s,r,n,a=l.querySelectorAll('iframe[data-secret=\"'+t.secret+'\"]'),o=l.querySelectorAll('blockquote[data-secret=\"'+t.secret+'\"]'),c=new RegExp(\"^https?:$\",\"i\"),i=0;i<o.length;i++)o[i].style.display=\"none\";for(i=0;i<a.length;i++)s=a[i],e.source===s.contentWindow&&(s.removeAttribute(\"style\"),\"height\"===t.message?(1e3<(r=parseInt(t.value,10))?r=1e3:~~r<200&&(r=200),s.height=r):\"link\"===t.message&&(r=new URL(s.getAttribute(\"src\")),n=new URL(t.value),c.test(n.protocol))&&n.host===r.host&&l.activeElement===s&&(d.top.location.href=t.value))}},d.addEventListener(\"message\",d.wp.receiveEmbedMessage,!1),l.addEventListener(\"DOMContentLoaded\",function(){for(var e,t,s=l.querySelectorAll(\"iframe.wp-embedded-content\"),r=0;r<s.length;r++)(t=(e=s[r]).getAttribute(\"data-secret\"))||(t=Math.random().toString(36).substring(2,12),e.src+=\"#?secret=\"+t,e.setAttribute(\"data-secret\",t)),e.contentWindow.postMessage({message:\"ready\",secret:t},\"*\")},!1)))}(window,document);\n\/\/# sourceURL=https:\/\/www.otava.com\/wp-includes\/js\/wp-embed.min.js\n\/* ]]> *\/\n<\/script>\n","description":"Join us for a free webinar on the FDA regulation of mHealth devices tomorrow at 2PM ET, with speakers Tatiana Melnik and Brian Balow of Dickinson Wright. When: June 5, 2012 @ 2 P.M. ET Where: Online &#8211; Register using GoToMeeting. Who: Tatiana Melnik, Attorney of Information Technology, Healthcare IT and Intellectual Property with Dickinson Wright; and Brian Balow, Partner at Dickinson Wright. What: FDA Regulation of Mobile Health Devices Description:\u00a0Software has increasingly become an integral part of healthcare, whether through incorporation into medical devices, as a stand-alone system that practitioners use to make clinical decisions, or as a means for transmitting and storing medical records. The federal government has supported the growth of mobile health technology through various incentives and directives, but the regulatory landscape remains unsettled. This presentation will review the Food and Drug Administration\u2019s approach to medical software regulation by providing a brief history, the FDA\u2019s current regulatory position, and where we anticipate the FDA will head in light of recent Congressional prodding. Recommended Reading: Mobile Health App Regulations: FDA &amp; HIPAA Keep ePHI on Secure Networks, Not Mobile Devices, Recommends OCR Mobile Security: Trying to Keep Up Tatiana Melnik, Attorney, Dickinson Wright PLLC Tatiana Melnik is...","thumbnail_url":"https:\/\/www.otava.com\/wp-content\/uploads\/2019\/04\/click-here-to-register.gif"}