PPD is the ideal consulting partner to assist with your biopharmaceutical product’s success from preclinical through post-approval.
Expedited recruitment, international regulatory expertise and operational teams trained in endocrine / metabolic indications.
PPD's Phase I clinic in Austin, Texas, conducts clinical studies to determine how new medicines act in the bodies of healthy volunteers. This is not testing to determine if the medicine works.
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Our dermatology study experience ranges from consulting on pre-investigational new drug (IND) briefing packages to preparing multiphase product development plans and from assembling new drug applications (NDAs) to providing biostatistical analyses.
We have conducted 861 clinical studies in dermatologic indications involving more than 20,025 patients and approximately 2,560 sites within the last five years.
We are experienced in clinical monitoring, clinical project management and market research. And we have been involved in various types of trials from small Phase I studies involving healthy volunteers to large, global, multicenter Phase III trials.
PPD has dermatology clinical research experience in a variety of areas including:
1Includes experience in hepatitis studies.
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