Phase II-IIIb Services
Our experience, support systems and infrastructure enable us to provide the highest level of program management and services for Phase II-IIIb clinical trials.
We offer:
- 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.
Drug & Product Development Consulting
Our strategic product development solutions staff helps our clients make the most cost-effective decisions throughout the development process, while our therapeutic consultants provide advice on drug development protocols and clinical trials.
Clinical Data Management
We have extensive data management experience for Phase I-IV clinical trials across a broad range of therapeutic areas and quantitative methods.
Clinical Quality Assurance
Our clinical quality assurance (CQA) staff helps our clients ensure clinical trials' integrity.
Clinical Project Management
Our project managers focus on providing on-time, on-cost quality deliverables.
Clinical Supply Management
We provide complete management of medical and pharmaceutical supplies through certified contract houses or PPD-owned distribution centers on behalf of our clients.
Clinical Trial Monitoring
Our dedicated clinical teams of skilled professionals provide consistent and effective monitoring and interaction with study sites.
Safety and Pharmacovigilance
We deliver medical and safety services according to comprehensive, customized safety plans.
Feasibility Studies
We provide comprehensive feasibility assessments and analysis to help our clients determine the most cost-effective and timely operational strategies for clinical trial or program execution.
Clinical Trial Patient Recruitment
Our experts attract qualified patients and shorten study enrollment timelines.
Clinical Biostatistics
We deliver accurate statistical analysis, reporting and high-quality output on time and within budget to satisfy our clients' needs.
Pharmacokinetic and Pharmacodynamic Support Services
We design and conduct clinical pharmacology protocols for expeditious review of submissions.
Regulatory Affairs
We guide our clients through the complexities of regulatory affairs with effective assessment and strategies to ensure a project progresses quickly and efficiently.
Medical Device Development
Our experienced medical device specialists provide innovative, results-focused support for our customers' clinical, regulatory and marketing needs.
Clinical Technology Services
Our appropriate and effective clinical trial technologies augment proven product development processes.
