Archives: Resources
Strategically Selecting the Right Sourcing Model for Study Management in Drug Development
This white paper shares insight on staffing models that can best maximize quality and efficiency during drug development changes.
Leveraging Digitally Reported Outcomes in Clinical Trials
PPD provides the leading expertise needed to support the implementation of digital solutions for clinical outcome assessments (COAs).
Post-Marketing Safety Registries
Learn how drug safety studies use cohort designs and retrospective data. Explore the benefits of post-marketing safety registries for regulatory planning.
Resource Options for the Evolving Needs of Emerging Biotechs
Watch a webinar to find out how PPD Biotech and PPD FSP work together to support our partners’ capacity planning and resource needs.
Protecting clinical research and patients through decentralized trial strategies
Read the article written by Alistair Davidson, Brittany Erana and Rhonda Henry, discussing how the success of clinical trials will depend on multi-platform solutions leveraging the latest technologies optimized for the specific requirements of the study and the needs of participants and stakeholders.
GMP Lab Capabilities and Services Overview
From pharmaceutical discovery through late stage research, clients benefit from our comprehensive GMP lab services.
Central Lab Capabilities Overview
PPD Laboratories combines world-class scientific expertise with state-of-the-art technologies supported by a commitment to exceptional quality.
Bioanalytical Lab Capabilities and Services Overview
Download the PPD Laboratories Bioanalytical Lab Capabilities and Services Overview.