Market Access & Communications

3 ways to incorporate DE&I in your communications strategy

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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Medical Communications Overview Brochure

Engaging those that matter most

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Lessons from China and the United States on the use of RWE in regulatory submissions

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Four reasons to conduct robust natural history studies before clinical trials

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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Can Synthetic / External Control Arms meet regulatory and HTA requirements?

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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Breaking through complex regulations and science speak – thinking “patients first” in lay language summary development

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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Evolution of Medical Communication Engagement

Our talented colleagues celebrate #MedComms Day as they talk through how the medical communications landscape was turned upside down for onsite meetings and scientific congresses last year and what th

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Importance of Diversity, Equity and Inclusion (DE&I) in medical communications

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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Strategies for External Control Arms

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Tips for building your oncology reimbursement strategy

In this infographic, we share five tips for building an effective reimbursement strategy for your oncology product.

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101 guide for real-world evidence

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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Payer insights for cell and gene therapies

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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Maximizing your virtual investigator meeting results

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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Impact of Real-World Evidence on Payers & Patients

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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Real-World Evidence: The Feedback Loop

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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Navigating the new normal for meetings – now and for the future

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Virtual meetings are easy, right?

Recommendations for navigating the "new normal" and how to prepare for the future.

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EMA Guidance: Management of Clinical Trials - What it means for Patients?

A lay summary for patients participating in clinical trials

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Putting the Pandemic in Plain Language

The COVID-19 pandemic has brought many negative feelings to the forefront of our everyday lives, including anxiety, fear and social division, but what if we explored the new positive relationships...

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CAR-T: How far have we come and where are we going?

In this episode, Doug Olson, one of the first CAR-T patients treated on a clinical trial for CLL almost 10 years ago, details his experiences with this therapy in its earliest days....

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Regulatory & Access Resources

Market Access & Communications