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Adverse Events Reporting in Clinical Trial Publications: MPIP Best Practice Recommendations

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Published on Dec 21, 2017

Jesse Berlin, ScD, VP and Global Head of Epidemiology, Johnson & Johnson, co-author of “Recommendations to Improve Adverse Event Reporting in Clinical Trial Publications: A Joint Pharmaceutical Industry/Journal Editor Perspective,” provides an insightful overview of this work (BMJ 2016;355:i5078). The recommendations provided in this publication help authors better identify, communicate, and display clinically relevant adverse event (AE) information.

By viewing this webinar, you will learn about:

· Insights gleaned from clinical investigators, journal editors, and biopharmaceutical industry experts involved in the reporting of AE data
· The importance of “clinical relevance” in AE reporting
· 5 best practice recommendations for AE reporting in medical publications, plus practical examples.
· How these recommendations complement existing guidelines for AE reporting

Insights and understanding gained from medical journal editors have been critical to driving improvements in transparency and credibility of industry-sponsored research publications. This webinar is part of an ongoing effort by MPIP to broaden the conversation and engage a wider audience in the effort to continue improvements and promote adoption of best practices.

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