RWE Summit 2019 Session

Real-world evidence on treatment outcomes can be an important aspect of the evidence basis for decision making if it is seen as credible. For real-world studies that are meant to test hypotheses about comparative-effectiveness or safety, a key aspect of credibility is that they are conducted transparently with tests that follow a prespecified analytic protocol. Preregistration of such study protocols on a public website would help build trust that their results can be used for decision-making purposes.

Establishing a Culture of Transparency for Real-World Evidence Studies...

The Real-World Evidence Transparency Initiative Partnership is a joint collaboration and ongoing effort between ISPOR, the International Society for Pharmacoepidemiology, the Duke-Margolis Center for Health Policy, and the National Pharmaceutical Council. The objective of this initiative is to establish a culture of transparency for study analysis and reporting of hypothesis evaluating real-world evidence studies on treatment effects.

 


 

Improving Transparency to Build Trust...

Value in HealthThe Real-World Evidence Transparency Initiative published a plan to encourage routine registration of noninterventional real-world evidence studies used to evaluate treatment effects. The report, “Improving Transparency to Build Trust in Real-World Secondary Data Studies for Hypothesis Testing—Why, What, and How: Recommendations and a Road Map from the Real-World Evidence Transparency Initiative,” was published in the September 2020 issue of Value in Health.


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The report, “Improving Transparency to Build Trust in Real-World Secondary Data Studies for Hypothesis Testing—Why, What, and How: Recommendations and a Road Map from the Real-World Evidence Transparency Initiative,” was published in the September 2020 issue of Value in Health. The plan includes specifying the rationale for registering hypothesis-evaluating treatment effectiveness real-world evidence studies, the studies that should be registered, where and when these studies should be registered, how and when analytic deviations from protocols should be reported, how and when to publish results, and incentives to encourage registration.

 


 

Real-World Evidence Registry

The Real-World Evidence Registry provides researchers with a fit-for-purpose platform to register their study designs before they begin work to facilitate the transparency needed to elevate the trust in the study results.

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Go To The Registry


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Real-world evidence studies can be used for hypothesis evaluation of treatment effects including safety (HETE studies). However these studies can also be perceived as less rigorous than clinical trials especially when not preregistered in a public setting such as ClinicalTrials.gov or the EU-PAS register.

ISPOR and its partners ISPE, NPC, and Duke Margolis have developed a simplified registration site especially for RWE HETE studies using secondary data. This searchable site provides a place for preregistration of studies that may not require registration for regulatory purposes but benefit from the rigor of transparent study methods and also provide a reference (such as a URL or doi) to share with peer reviewers, assessors, or other decision making bodies. Researchers can get started ‘here’ by creating a profile on the Open Sciences Framework and registering their study on the RWE Registry.

 


 

Shaking the Myth of Real-World Evidence

On-Demand Webinar

Learn more by watching the on-demand webinar, “Shaking the Myth of Real-World Evidence: Updates from the RWE Transparency Initiative.” This session provides updates from the initiative including a walk-through of the study registration site and updates on the special task force developing a standardized RWE protocol template.

View Webinar

Download Slides

 
 
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Conferences & Summits 

November 17: Developing Decision-Grade Real-World Evidence - In Person at ISPOR Europe 2024
event-Short-Courses

November 17, 2024

<p><a href="/education-training/short-courses">Back to all short courses</a><br /></p><p><strong>Developing Decision-Grade Real-World Evidence (in person)</strong><br /><strong><br />LEVEL:&nbsp;</strong>Intermediate<strong><br />TRACK:&nbsp;</strong>Real World Data &amp; Information Systems<strong><br />LENGTH: </strong>4<strong>&nbsp;</strong>Hours | Course runs 1 day<br /><br />This short course is offered in-person at the ISPOR Europe 2024 conference. Separate registration is required.&nbsp; <a href="/conferences-education/conferences/upcoming-conferences/ispor-europe-2024">Visit the ISPOR Europe 2024 Program page to register</a>&nbsp;and learn more.<br /></p><p><strong><strong>Sunday, 17 November 2024 | Course runs 1 Day<br /></strong></strong>08:00-12:00 Central European Time (CET)&nbsp;<br /><strong><br />DESCRIPTION</strong></p><div>Separate registration required.</div><div fontscheme-block="2"><br /></div><div>In this course, participants will be introduced to the principles of what makes real-world evidence (RWE) decision-grade, including an extended example. In the first half of the course, will review the most recent RWE frameworks and guidelines, and examine case studies in which RWE was used in regulatory and HTA approval. The second half of the course is an extended example in which participants will examine a study that could support an indication expansion, and interactively discuss how choices made in the design and implementation may affect the meaning and interpretability of results.</div><div></div><div><strong fontscheme="2">PREREQUISITE: </strong>Students are expected to be familiar with relevant concepts and methodologies for analyzing real-world data.</div><p></p><p><strong></strong><strong>FACULTY MEMBERS</strong><strong></strong></p><div><strong></strong></div><div><strong></strong></div><div><strong></strong></div><div><strong>Sebastian Schneeweiss, MD, ScD</strong></div><div>Professor of Medicine and Epidemiology, Harvard Medical School </div><div>and Chief, Division of Pharmacoepidemiology </div><div>Brigham and Women&rsquo;s Hospital</div><div>Boston, MA, USA</div><div bold-block="true"><br /></div><div><strong>Jeremy A. Rassen, ScD</strong></div><div>Co-Founder &amp; Chief Scientific Officer</div><div>Aetion, Inc.</div><div>New York, NY, USA</div><div><br /></div><div><strong>Shirley Wang, PhD</strong></div><div>Associate Professor of Medicine </div><div>Division of Pharmacoepidemiology and Pharmacoeconomics</div><div>Department of Medicine, Brigham and Women&rsquo;s Hospital</div><div>Harvard Medical School</div><div>Boston, MA, USA</div><div></div><div><p><strong style="background-color:transparent;color:inherit;font-size:inherit;text-align:inherit;text-transform:inherit;word-spacing:normal;caret-color:auto;white-space:inherit;">&nbsp;</strong></p><p><strong style="background-color:transparent;color:inherit;font-size:inherit;text-align:inherit;text-transform:inherit;word-spacing:normal;caret-color:auto;white-space:inherit;">Basic Schedule:</strong><br /></p></div><p>4 Hours | Course runs 1 Day</p>)

Short Courses & Webinars 

November 17: Developing Decision-Grade Real-World Evidence - In Person at ISPOR Europe 2024
event-Short-Courses

November 17, 2024

<p><a href="/education-training/short-courses">Back to all short courses</a><br /></p><p><strong>Developing Decision-Grade Real-World Evidence (in person)</strong><br /><strong><br />LEVEL:&nbsp;</strong>Intermediate<strong><br />TRACK:&nbsp;</strong>Real World Data &amp; Information Systems<strong><br />LENGTH: </strong>4<strong>&nbsp;</strong>Hours | Course runs 1 day<br /><br />This short course is offered in-person at the ISPOR Europe 2024 conference. Separate registration is required.&nbsp; <a href="/conferences-education/conferences/upcoming-conferences/ispor-europe-2024">Visit the ISPOR Europe 2024 Program page to register</a>&nbsp;and learn more.<br /></p><p><strong><strong>Sunday, 17 November 2024 | Course runs 1 Day<br /></strong></strong>08:00-12:00 Central European Time (CET)&nbsp;<br /><strong><br />DESCRIPTION</strong></p><div>Separate registration required.</div><div fontscheme-block="2"><br /></div><div>In this course, participants will be introduced to the principles of what makes real-world evidence (RWE) decision-grade, including an extended example. In the first half of the course, will review the most recent RWE frameworks and guidelines, and examine case studies in which RWE was used in regulatory and HTA approval. The second half of the course is an extended example in which participants will examine a study that could support an indication expansion, and interactively discuss how choices made in the design and implementation may affect the meaning and interpretability of results.</div><div></div><div><strong fontscheme="2">PREREQUISITE: </strong>Students are expected to be familiar with relevant concepts and methodologies for analyzing real-world data.</div><p></p><p><strong></strong><strong>FACULTY MEMBERS</strong><strong></strong></p><div><strong></strong></div><div><strong></strong></div><div><strong></strong></div><div><strong>Sebastian Schneeweiss, MD, ScD</strong></div><div>Professor of Medicine and Epidemiology, Harvard Medical School </div><div>and Chief, Division of Pharmacoepidemiology </div><div>Brigham and Women&rsquo;s Hospital</div><div>Boston, MA, USA</div><div bold-block="true"><br /></div><div><strong>Jeremy A. Rassen, ScD</strong></div><div>Co-Founder &amp; Chief Scientific Officer</div><div>Aetion, Inc.</div><div>New York, NY, USA</div><div><br /></div><div><strong>Shirley Wang, PhD</strong></div><div>Associate Professor of Medicine </div><div>Division of Pharmacoepidemiology and Pharmacoeconomics</div><div>Department of Medicine, Brigham and Women&rsquo;s Hospital</div><div>Harvard Medical School</div><div>Boston, MA, USA</div><div></div><div><p><strong style="background-color:transparent;color:inherit;font-size:inherit;text-align:inherit;text-transform:inherit;word-spacing:normal;caret-color:auto;white-space:inherit;">&nbsp;</strong></p><p><strong style="background-color:transparent;color:inherit;font-size:inherit;text-align:inherit;text-transform:inherit;word-spacing:normal;caret-color:auto;white-space:inherit;">Basic Schedule:</strong><br /></p></div><p>4 Hours | Course runs 1 Day</p>)

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