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<h1>Events</h1>
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<h2>ABS/AACT Educational Workshop: Getting More Out of Your Post-Marketing Registry</h2>
<h3>February 27 – 29, 2008<br>Florida</h3>
<h3>Abt Associates was an Event Sponsor</h3>
<p>Phase IV is the fastest-growing area of clinical research today. Due to timeline and budget constraints, the Phase IV process has been becoming an issue of concern to the drug development industry. With an ever changing regulatory environment, continual concerns about the safety of new medicines, and various uses for large-scale, real-world data on marketed drugs', safety and efficacy are primary drivers of the growth seen in the Phase IV research environment today.</p>
<p>Post-marketing research is always an important element of commercialization that enables companies to expand existing markets, enter new markets, develop and deliver messaging that directly compares their products with the competition, and secure a niche position in crowded marketing. This conference examined the critical challenges the post-marketing research industry has been facing and offered a variety of industry knowledge seeking to secure Phase IV clinical safety, efficiency and cost-effectiveness.</p>
<h3>Key Topics</h3>
<ul><li>Updates on the Impact of FDA and FDAAA on Phase IV Studies</li>
<li>Prioritizing Phase IV while Aligning with your Company's Goals</li>
<li>Analyzing Investigator Initiated Studies and their Impact on Phase IV Clinical Trials</li>
<li>Conducting Phase IV Clinical Trials in a Changing Drug Environment</li>
<li>Investigating the Legal Implications and Risks within Phase IV</li></ul>
<h3>Abt Associates Clinical Trials (AACT) offered a workshop:</h3>
<p><strong>Getting More Out of Your Post-Marketing Registry</strong>
<br />
There has been much in the news about the ever-increasing reliance on post-marketing registries to satisfy a growing list of regulatory, safety, and reimbursement commitments. These external demands have broadened the number of stakeholders within sponsor organizations, each with a distinct expectation of what a registry will deliver for them. The goals of this dynamic workshop were:</p>
<ul><li>To take a bird's eye view of the recent legislation that provides the FDA with broader powers to ensure the safety of prescription drug products</li>
<li>To hear from your colleagues how this new legislation is being interpreted and acted upon among sponsor companies</li>
<li>To explore the opportunities the new legislation presents to sponsors in designing a multifaceted registry program</li>
<li>To assess the numerous choices and trade-offs while devising successful registry design and implementation strategies</li>
<li>To identify the benefits of planning for these post-marketing demands well before formal market approval</li>
</ul>
<p>For more information about the conference visit the <a href="http://www.marcusevans.com/html/eventdetail.asp?eventID=13597&SectorID=31&pageID=0" target="_blank">6th Annual Phase IV Clinical Trials Conference website</a>. For more information regarding Abt Associates' workshop, or our registry capabilities:</p>
<h3>Contact</h3>
<p><a href="mailto:[email protected]">[email protected]</a>
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