{"version":"1.0","provider_name":"AST, Inc.","provider_url":"https:\/\/www.ast-inc.com","author_name":"Colin Kish","author_url":"https:\/\/www.ast-inc.com\/author\/extract-marketing-group\/","title":"Quality by Design: Principles & Considerations | AST","type":"rich","width":600,"height":338,"html":"<blockquote class=\"wp-embedded-content\" data-secret=\"19FHCjGpZy\"><a href=\"https:\/\/www.ast-inc.com\/blogs\/pharmaceutical-development-quality-by-design-principles-and-considerations-part-1\/\">Quality by Design: Principles and Considerations<\/a><\/blockquote><iframe sandbox=\"allow-scripts\" security=\"restricted\" src=\"https:\/\/www.ast-inc.com\/blogs\/pharmaceutical-development-quality-by-design-principles-and-considerations-part-1\/embed\/#?secret=19FHCjGpZy\" width=\"600\" height=\"338\" title=\"&#8220;Quality by Design: Principles and Considerations&#8221; &#8212; AST, Inc.\" data-secret=\"19FHCjGpZy\" frameborder=\"0\" marginwidth=\"0\" marginheight=\"0\" scrolling=\"no\" class=\"wp-embedded-content\"><\/iframe><script>\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.ast-inc.com\/wp-includes\/js\/wp-embed.min.js\n<\/script>\n","thumbnail_url":"https:\/\/www.ast-inc.com\/wp-content\/uploads\/2025\/07\/New-Gen-R-FCM-1-1.jpg","thumbnail_width":1770,"thumbnail_height":976,"description":"The following article is\u00a0part 1\u00a0of a blog series that has been adapted from Principal Commissioning, Qualification and Validation Engineer Jason Rossi\u2019s recent article in\u00a0Cleanroom Technology. In the world of pharmaceutical development, the journey of the drug product to commercialization is largely defined by a single word: quality. A key point that\u2019s clear in the revised [&hellip;]"}