PPD’s endocrinology and metabolic clinical trial experience helps us to manage programs of any size and complexity around the world.
PPD conducts clinical trials around the world that involve the testing of new drugs or delivery methods to determine safety and effectiveness.
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We are the right partner to help you progress along the path of drug development and market access by using the right expertise, the right patients, the right sites and the right evidence. Whether you are in preclinical planning or post-approval management, we will work closely with you to develop and execute customized plans that increase efficiency and reduce risks to your portfolio to help you achieve sweet success.
PPD, including Evidera, our peri- and post-approval business unit, provides you industry-leading expertise across the drug development process. With a focus on innovation, we work to enable advances in clinical development and evidence generation to create tailored solutions for your specific product challenges. Together, we leverage our insights and expertise to help you advance your products to market quickly and successfully.
Reaching patients is the foundation of PPD’s mission to deliver life-changing therapies. We meet your aggressive enrollment and retention goals through customized patient and site strategies. Through our industry partnerships and business units, PPD offers access to 200+ million identifiable lives and 170+ million de-identified lives. Through our Accelerated Enrollment Solutions (AES) business unit, PPD offers best-in-class site and enrollment solutions through industry leaders Synexus, Acurian and Optimal Research.
With comprehensive evidence-based solutions to demonstrate real-world effectiveness, safety and value, Evidera, PPD’s peri- and post-approval business unit, provides integrated scientific expertise with global operational capabilities to deliver the evidence needed to optimize the market access and commercial potential of your products.
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