Communicating Value to Providers and Payers
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Read five ways biotech companies can enhance their value story with advanced analytics.
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In this infographic, we outline three ways to incorporate Diversity, Equity and Inclusion into your strategy to deliver inclusive communications that connect with a diverse and multicultural audience
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Engaging those that matter most
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Lucas Kempf, former regulator, reflects on his time at the FDA and outlines why companies should invest in a high-quality natural history study.
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This article summarizes a recent panel discussion where experts from Parexel and biotech company, MorphoSys, shared their experiences from recent pioneering efforts in RWE.
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In this blog, our experts explore how to develop multi-purpose, patient-centric lay language summaries with the patient audience firmly in mind.
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Parexel colleagues celebrate #MedComms Day as they talk through how the medical communications landscape was turned upside down for onsite meetings and scientific congresses in 2020 and what this mean
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Parexel communications experts celebrate #MedComms day by discussing how new guidelines and changes in the clinical trial space translate to medical communications and how Parexel plans to approach fu
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In this infographic, we share five tips for building an effective reimbursement strategy for your oncology product.
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We have created this guide to simplify the terminology of real-world evidence (RWE) and outline some of the strategic options available.
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Emma Medin, VP, Pricing & Market Access, shares three payer insights to help you price appropriately for your cell or gene therapy.
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Learn how Parexel brings the principles and energy from face-to-face investigator meetings to an interactive and engaging virtual environment.
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Dr. Scott Gottlieb, Former Commissioner of the Food and Drug Administration speaks with Parexel’s Peyton Howell, Executive Vice President, Chief Commercial & Strategy Officer and Sy Pretorius, Executi
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RWE experts Leanne Larson, Senior Vice President and Worldwide Head, Real-World Evidence and Access and Amy McKee, Vice President, Regulatory and Access dig deeper into the evolving role of RWE.
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Recommendations for navigating the "new normal" and how to prepare for the future.
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A lay summary for patients participating in clinical trials
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