PPD brings extensive experience in the nuances of post-approval studies, combined with a solid foundation in late-stage clinical trials management.
Extensive knowledge of hematology and oncology research, vast capabilities and experience with feasibility studies and a large investigator network.
PPD's Phase I Clinic conducts clinical studies to determine how new medicines act in the bodies of healthy volunteers.
PPD News and Events Media kit
In the first of a four-part series, Jai Balkissoon, vice president of global product development, writes about the increase in immuno-oncology therapies.
Alistair Davidson, senior director, regulatory affairs, discusses the work of local regulatory affiliates.
As we recognize World TB (tuberculosis) Day, PPD employees share their experiences working against the disease and their dedication to seek life-changing therapies for TB patients.
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.
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