Where better medicines begin_Early Phase ebook 2022

Are you using RWE? ebook

Are you using real-world evidence? RWE strategies span the development lifecycle.

The upward trend of FSP outsourcing

Data Linking in Clinical Trials

mHealth Innovation_Identifying the Best Patient-Centered Tech for Clinical Trials

mHealth Innovation - identify the best patient-centered tech webinar slides_Parexel_ActiGraph

Preparing for Our Risk-based Future: Using Change Management to Drive RBQM Adoption

Master Protocols from Design to Delivery

This whitepaper discusses the changes in master protocols within the clinical research community and walks through best practices on how to address the changes.

Preparing for a Risk-based Future

Landing in the EU – The importance of choosing the right experts for EU/EEA QPPV

Embarking on the Next Era of Precision Medicine

In this article Angela Qu, M.D., Ph.D., Vice President, Biomarkers and Genomic Medicine, discusses the pan-cancer drug development approach guided by biomarkers.

Putting AI to Work in Your Safety Program

This article discusses the increasing use of AI in pharmacovigilance activities to increase efficiency and outcomes as data volume continues to increase.

How to Accelerate Oncology Clinical Trials through Site Relationships and Patient Insights

Learn how all stakeholders benefit when patients and their insights are at the heart of every aspect of clinical development.

Decentralized clinical trials - A more patient-centric approach

Decentralized clinical trials, where portions of a study are conducted outside a traditional trial site, offer new opportunities — and new hope — for patients struggling with inflammatory conditions.

COVID-19 vaccine signal detection study

Entering a new age of evidence generation: synthetic control models

Expert perspectives from Parexel's Leanne Larson, Senior Vice President and WW Head of Real-World Evidence

Regulatory, clinical and logistics challenges of ATMPs in clinical research

This article explores the nature and manufacturing process of ATMP and how clinical professionals can execute the development and marketing of these therapies.

IDMP integrity

This article provides insight into how clinical research organizations can carefully create robust planning and optimization solutions with IDMP integrity in mind.

Preparing for the journey

There are challenges at every point in the clinical supply chain process. This article reviews the risks associated with the planning and execution of a clinical site supply strategy.

Fact Sheet: Accelerate Clinical Development through enhanced biologic management

Learn how Parexel accelerates clinical development through enhanced biologic management—and our steps in supporting our clients and patients along the way.