Our experience, support systems and infrastructure enable us to provide the highest level of program management and clinical development services for Phase II-IIIb clinical trials.
- Global infrastructure and support
- Quality processes and accurate reporting
- Regulatory expertise
We advance a product through development and approval on time and within a client's budget. Our experienced teams deliver quality results for our clients' drug research and development needs.
Project managers focus on providing on-time, on-budget, quality deliverables.
PPD has developed a novel approach to accessing sites and patients — a new approach, grounded in clinical innovation, that puts the focus on patients.
Dedicated teams of professionals provide consistent and effective monitoring and interaction with study sites.
PPD is advancing clinical research through the innovative data and analytics platform Preclarus.®
Expertise in data management for Phase I-IV clinical trials across all therapeutic areas and quantitative methods.
Deliver accurate statistical analysis, reporting and high-quality output on time and within budget to our clients.
Our global pharmacovigilance team is comprised of physicians, pharmacists and other medically trained professionals.
Learn more about how PPD FSP can deliver across a broad range of service areas
Guide our clients through the complexities of regulatory affairs with effective assessment and strategies to ensure rapid and efficient project progression.
Clinical quality assurance (CQA) staff helps our clients ensure clinical trial integrity.
Our dedicated team of experienced professionals delivers IRT system services to clients.
Provides complete management of medical and pharmaceutical supplies through certified contract houses or PPD-owned distribution centers.