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  235.          <div class="abstract">For two decades, Drug GMP Report has provided thorough analysis and interpretation of current good manufacturing practice (cGMP) regulations, FDA enforcement trends and warning letters, international regulations and more. It’s like receiving a monthly executive briefing packed with the latest on inspection hot spots, developments in international harmonization efforts, electronic data requirements and evolving trends in cGMP enforcement. Plus, every issue, you get links to critical documents such as draft and final guidances, Form 483s, warning letters, proposed rules, full text of proposed legislation and a host of others.</div>
  236.        </div>
  237.        <div class="record">
  238.          <h2 class="headline"><a title="Drug Industry Daily" href="https://www.fdanews.com/rss/13">Drug Industry Daily</a></h2>
  239.          <div class="abstract">This daily electronic briefing delivers coverage of what’s happening on Capitol Hill and at the FDA, FTC, HHS and other key agencies and decision-making bodies that affect the pharmaceutical industry. Each issue gives you hard reporting on top issues, such as patent exclusivity, market globalization, biosimilar development, advertising, program funding, FDA appropriations, warning letters, recalls, approvals and more. Written by FDAnews’ veteran staff of reporters, you get the latest news with the added perspective that only seasoned reporters can provide. It’s the fastest, most reliable way to make sure you’re an industry expert.</div>
  240.        </div>
  241.        <div class="record">
  242.          <h2 class="headline"><a title="International Devices &amp; Diagnostics Letter Monitor" href="https://www.fdanews.com/rss/28">International Devices &amp; Diagnostics Letter Monitor</a></h2>
  243.          <div class="abstract">International Devices & Diagnostics Monitor (IDDM) is a one-stop resource that brings you a complete, global picture of the medical device regulations that affect your business. Nowhere else will you find a more comprehensive collection of all the regulatory changes in the US, EU, Asia, Latin America, the Middle East, Australia and the rest of the world. Your subscription includes a weekly newsletter to keep you up to date with global regulations as changes happen, including complete text of all government documents. </div>
  244.        </div>
  245.        <div class="record">
  246.          <h2 class="headline"><a title="Generic Line" href="https://www.fdanews.com/rss/14">Generic Line</a></h2>
  247.          <div class="abstract">For over 25 years, the Generic Line has been the leading resource for accurate, up-to-date analysis of FDA policies affecting generic drugs and drug patents. With a new biosimilars approval path, blockbuster drugs facing patent cliffs, and the FTC trying to stop pay-for-delay agreements, there's never been a more critical time to subscribe. With every issue, you get links to additional key documents, such as FDA guidances, warning letters, rules, full texts of proposed legislation and much more.</div>
  248.        </div>
  249.        <div class="record">
  250.          <h2 class="headline"><a title="International Pharmaceutical Regulatory Monitor" href="https://www.fdanews.com/rss/16">International Pharmaceutical Regulatory Monitor</a></h2>
  251.          <div class="abstract">International Pharmaceutical Regulatory Monitor has been a ‘must read’ for pharma professionals for more than 40 years, bringing them the latest changes in rules and standards at the FDA, European Medicines Agency, Health Canada, Australia's TGA, International Conference on Harmonisation and other key organizations. And as the global marketplace has expanded to markets in Latin America, Asia and Africa, IPRM has kept readers informed of regulatory developments in those regions as well. In each issue, you get actual English-language texts of important, hard-to-obtain proposals, regulations, guidances and other documents to help ensure speedy reviews of your regulatory submissions and success at home and abroad.</div>
  252.        </div>
  253.        <div class="record">
  254.          <h2 class="headline"><a title="The GMP Letter" href="https://www.fdanews.com/rss/18">The GMP Letter</a></h2>
  255.          <div class="abstract">For 30 years, medical device manufacturers worldwide have relied on The GMP Letter to comply with the FDA's interpretation and enforcement of cGMPs and the Quality System Regulation (QSR). In each issue, you get an update on regulations and guidances and learn which companies the FDA has inspected and what the audits revealed. You also get links to Form 483s, warning letters, closeout letters, FDA policy notices and many other reports to help make your quality assurance efforts a success.</div>
  256.        </div>
  257.        <div class="record">
  258.          <h2 class="headline"><a title="FDAnews Device Daily Bulletin" href="https://www.fdanews.com/rss/5">FDAnews Device Daily Bulletin</a></h2>
  259.          <div class="abstract">Each day you'll receive targeted FDA regulatory, legislative and business news briefs in the pharmaceutical and biologics industries. Plus, you'll get a snapshot of international news relevant to your business. In just a few minutes you can scan major headlines and click through to read the stories you want. Sign up today and receive your first FDAnews Drug Daily Bulletin the next business day. This subscription includes a weekly email alert, FDAnews' Pharma Solution of the Week, highlighting one problem and one solution in the pharmaceutical arena.</div>
  260.        </div>
  261.        <div class="record">
  262.          <h2 class="headline"><a title="FDAnews Drug Daily Bulletin" href="https://www.fdanews.com/rss/7">FDAnews Drug Daily Bulletin</a></h2>
  263.          <div class="abstract">Each day you'll receive targeted FDA regulatory, legislative and business news briefs in the pharmaceutical and biologics industries. Plus, you'll get a snapshot of international news relevant to your business. In just a few minutes you can scan major headlines and click through to read the stories you want. Sign up today and receive your first FDAnews Drug Daily Bulletin the next business day. This subscription includes a weekly email alert, FDAnews' Pharma Solution of the Week, highlighting one problem and one solution in the pharmaceutical arena.</div>
  264.        </div>
  265.        <div class="record">
  266.          <h2 class="headline"><a title="QMN Weekly Bulletin" href="https://www.fdanews.com/rss/25">QMN Weekly Bulletin</a></h2>
  267.          <div class="abstract">By reading the Quality Management Network's QMN Weekly Bulletin you can keep track of the latest from the FDA, Congress and industry experts in the world of cGMP's for pharmaceutical and medical device manufacturers. Each issue delivers crucial information on regulatory changes and inspection trends, as well as a wrap-up of the major quality management news from around the world. Sign up today and start receiving The QMN Weekly Bulletin.</div>
  268.        </div>
  269.    </div>
  270.    <div class="records topic-feeds">
  271.      <h3 class="topic-feeds__title">Topic Feeds</h3>
  272.      <div class="topic-feeds__list">
  273.          <div class="record topic-feed-item">
  274.            <h2 class="headline topic-feed-item__headline">
  275.              <a title="Commercial Operations" href="https://www.fdanews.com/rss/topic/118-commercial-operations">Commercial Operations</a>
  276.            </h2>
  277.          </div>
  278.          <div class="record topic-feed-item">
  279.            <h2 class="headline topic-feed-item__headline">
  280.              <a title="GMPs" href="https://www.fdanews.com/rss/topic/116-gmps">GMPs</a>
  281.            </h2>
  282.          </div>
  283.          <div class="record topic-feed-item">
  284.            <h2 class="headline topic-feed-item__headline">
  285.              <a title="Inspections and Audits" href="https://www.fdanews.com/rss/topic/117-inspections-and-audits">Inspections and Audits</a>
  286.            </h2>
  287.          </div>
  288.          <div class="record topic-feed-item">
  289.            <h2 class="headline topic-feed-item__headline">
  290.              <a title="Postmarket Safety" href="https://www.fdanews.com/rss/topic/120-postmarket-safety">Postmarket Safety</a>
  291.            </h2>
  292.          </div>
  293.          <div class="record topic-feed-item">
  294.            <h2 class="headline topic-feed-item__headline">
  295.              <a title="Quality" href="https://www.fdanews.com/rss/topic/114-quality">Quality</a>
  296.            </h2>
  297.          </div>
  298.          <div class="record topic-feed-item">
  299.            <h2 class="headline topic-feed-item__headline">
  300.              <a title="Regulatory Affairs" href="https://www.fdanews.com/rss/topic/115-regulatory-affairs">Regulatory Affairs</a>
  301.            </h2>
  302.          </div>
  303.          <div class="record topic-feed-item">
  304.            <h2 class="headline topic-feed-item__headline">
  305.              <a title="Research and Development" href="https://www.fdanews.com/rss/topic/108-research-and-development">Research and Development</a>
  306.            </h2>
  307.          </div>
  308.          <div class="record topic-feed-item">
  309.            <h2 class="headline topic-feed-item__headline">
  310.              <a title="Submissions and Approvals" href="https://www.fdanews.com/rss/topic/109-submissions-and-approvals">Submissions and Approvals</a>
  311.            </h2>
  312.          </div>
  313.          <div class="record topic-feed-item">
  314.            <h2 class="headline topic-feed-item__headline">
  315.              <a title="Commercial Operations" href="https://www.fdanews.com/rss/topic/127-commercial-operations">Commercial Operations</a>
  316.            </h2>
  317.          </div>
  318.          <div class="record topic-feed-item">
  319.            <h2 class="headline topic-feed-item__headline">
  320.              <a title="Inspections and Audits" href="https://www.fdanews.com/rss/topic/126-inspections-and-audits">Inspections and Audits</a>
  321.            </h2>
  322.          </div>
  323.          <div class="record topic-feed-item">
  324.            <h2 class="headline topic-feed-item__headline">
  325.              <a title="Postmarket Safety" href="https://www.fdanews.com/rss/topic/129-postmarket-safety">Postmarket Safety</a>
  326.            </h2>
  327.          </div>
  328.          <div class="record topic-feed-item">
  329.            <h2 class="headline topic-feed-item__headline">
  330.              <a title="Quality" href="https://www.fdanews.com/rss/topic/123-quality">Quality</a>
  331.            </h2>
  332.          </div>
  333.          <div class="record topic-feed-item">
  334.            <h2 class="headline topic-feed-item__headline">
  335.              <a title="Regulatory Affairs" href="https://www.fdanews.com/rss/topic/124-regulatory-affairs">Regulatory Affairs</a>
  336.            </h2>
  337.          </div>
  338.          <div class="record topic-feed-item">
  339.            <h2 class="headline topic-feed-item__headline">
  340.              <a title="Research and Development" href="https://www.fdanews.com/rss/topic/121-research-and-development">Research and Development</a>
  341.            </h2>
  342.          </div>
  343.          <div class="record topic-feed-item">
  344.            <h2 class="headline topic-feed-item__headline">
  345.              <a title="Submissions and Approvals" href="https://www.fdanews.com/rss/topic/122-submissions-and-approvals">Submissions and Approvals</a>
  346.            </h2>
  347.          </div>
  348.          <div class="record topic-feed-item">
  349.            <h2 class="headline topic-feed-item__headline">
  350.              <a title="QSR" href="https://www.fdanews.com/rss/topic/125-qsr">QSR</a>
  351.            </h2>
  352.          </div>
  353.          <div class="record topic-feed-item">
  354.            <h2 class="headline topic-feed-item__headline">
  355.              <a title=" FDA Enforcement Actions" href="https://www.fdanews.com/rss/topic/263-fda-enforcement-actions"> FDA Enforcement Actions</a>
  356.            </h2>
  357.          </div>
  358.          <div class="record topic-feed-item">
  359.            <h2 class="headline topic-feed-item__headline">
  360.              <a title="Legislative Update" href="https://www.fdanews.com/rss/topic/260-legislative-update">Legislative Update</a>
  361.            </h2>
  362.          </div>
  363.          <div class="record topic-feed-item">
  364.            <h2 class="headline topic-feed-item__headline">
  365.              <a title="Meeting Planner" href="https://www.fdanews.com/rss/topic/261-meeting-planner">Meeting Planner</a>
  366.            </h2>
  367.          </div>
  368.          <div class="record topic-feed-item">
  369.            <h2 class="headline topic-feed-item__headline">
  370.              <a title="Quick Notes" href="https://www.fdanews.com/rss/topic/266-quick-notes">Quick Notes</a>
  371.            </h2>
  372.          </div>
  373.          <div class="record topic-feed-item">
  374.            <h2 class="headline topic-feed-item__headline">
  375.              <a title="Regulatory Update" href="https://www.fdanews.com/rss/topic/262-regulatory-update">Regulatory Update</a>
  376.            </h2>
  377.          </div>
  378.          <div class="record topic-feed-item">
  379.            <h2 class="headline topic-feed-item__headline">
  380.              <a title="COVID-19" href="https://www.fdanews.com/rss/topic/230-covid-19">COVID-19</a>
  381.            </h2>
  382.          </div>
  383.      </div>
  384.    </div>
  385. </div>
  386. </div>
  387. <div class="main-interior-sidebar"><section class="upcoming-events ">
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