Find out how PPD’s clinical development services can help advance drug research and development for your product.
PPD’s endocrinology and metabolic clinical trial experience helps us to manage programs of any size and complexity around the world.
PPD’s Las Vegas clinical research unit recruits clinical trial volunteers for a wide range of studies.
PPD News and Events Media kit
PPD employees, including a rare disease patient, parent and researcher, share their experiences as we honor Rare Disease Day.
Nicole Stansbury, executive director of adaptive and intelligent monitoring, answers questions about PPD’s clinical trial monitoring strategies.
Brent Reed, director of information technology, writes about elements required for managing data for a successful clinical trial.
Chris Forsdyke, executive director, PPD® Laboratories’ GMP lab in Athlone, Ireland, details why proactivity is important even in a regulated laboratory environment.
Andres Bayona, executive director in clinical monitoring and regional head of Latin America, and Mercedes Ponce de Leon, senior manager in regulatory affairs, discuss the clinical trial regulatory landscape in Latin America.
Jie Ding, associate director of development and validation at the PPD® Laboratories’ GMP lab, discusses liquid chromatography-mass spectrometry in drug discovery and development.
Kirsten Messmer, Ph.D., R.A.C., principal regulatory affairs specialist, details changes in regulatory guidelines for first-in-human trials.
Stephen Peroutka, vice president and therapeutic area head in neuroscience, shares his thoughts on the importance and outlook of conducting clinical trials for Alzheimer’s disease.
Regulatory affairs experts at PPD, Alistair Davidson and Vincenzo Cannizzaro, reflect on how the United Kingdom's departure from the European Union might impact the pharmaceutical industry.
Bill Wang, director of regulatory affairs, discusses China's regulatory environment in the second-largest pharmaceutical market in the world.
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