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Patient Studies
PPD’s extensive experience in Phase II-IIIb trials can be tailored to the unique needs of early phase clinical development programs. Our clinical, scientific, regulatory and professional staff delivers integrated and effective planning and implementation for patient studies beginning in Phase I and proceeding seamlessly into subsequent phases.
Global Clinical Capabilities
Mobilization of global clinical resources and integrated processes will help you bring your product to market faster. We provide services specific to each client’s unique needs, as well as work within global standard operating procedures. A master action plan tailored to the needs of each project includes:
- Transfer of obligations
- Clinical operations
- Data management and biostatistics
- Medical writing
- Quality management
Services:
Project Management
Clinical Monitoring
Data Management
Biostatistics
Safety and Pharmacovigilance
Regulatory Affairs
Patient Recruitment
Technology Services
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