275 Grove St., Suite 101C, Newton, MA 02466
+1 617 454 9300
2520 Meridian Parkway, Research Triangle Park, Suite 200, Durham, NC 27713
+1 919 544 3170
© 2000-2022. Parexel International Corporation.
275 Grove St., Suite 101C, Newton, MA 02466
+1 617 454 9300
2520 Meridian Parkway, Research Triangle Park, Suite 200, Durham, NC 27713
+1 919 544 3170
© 2000-2022. Parexel International Corporation.
Communicating the value of your drug by presenting clinical results through peer-reviewed publications is fundamental to your success and developing a strong publications strategy requires experienced planners who understand your goals and your audiences’ needs. Our full-time medical writers and editors have decades of experience covering all major therapeutic areas and rare disease types. Parexel’s highly experienced team can build a strategic publication plan that integrates your needs and goals, as well as identification of key congresses and medical journals in collaboration with authors. We then compliantly help navigate the submission and peer-review process to achieve rapid, compelling, and efficient publication.
With over 30 years of experience in strategic publication planning across many therapeutic areas, Parexel is a publications powerhouse. Our digital publication and congress solutions help companies engage and inspire audiences, streamlining complex data and measuring impact – all powered by our expert team, many of whom are active members of the International Society of Medical Publication Professionals (ISMPP).
At Parexel, we don’t just develop publications with our best minds, we create them with our big hearts. This is demonstrated by applying health and patient literacy guidelines to patient-focused materials and our defined process for developing plain language summaries.
Pharma medical lead:
"Thanks very much for your help in putting together not only this abstract and the paper, but also all of the other abstract, posters, and manuscripts that you have worked on for the project. I expect that without your help, only a small fraction of what you
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Preparedness for the Clinical Trials Regulation (EU) 536/2014 will require a wide-ranging cross enterprise business strategy including for both ongoing and new clinical trials to be set up correctly. Are you ready for the change? Download our factsheet to learn more about how Parexel can help you prepare for the transition.
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