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Site and Patient Centric Solutions
PPD has developed a novel approach to accessing sites and patients.
How an FSP Model Can Ensure Business Continuity During a Business Disruption
Explore FSP rebadging to address staffing challenges amid business disruptions in a way that mutually benefits both your business and your employees.
Three Important Considerations in Operationalizing Nonalcoholic Steatohepatitis (NASH) Global Trials
Our experts discuss solutions to three common challenges worth considering when operationalizing global NASH clinical trials.
A Drug Development Guide for Cell and Gene Therapies
Our expert team details unique considerations and strategies for the development of cell and gene therapies.
GMP Lab Capabilities
Learn more about the capabilities PPD Laboratory Services’ GMP lab offers to meet customers’ needs from cell-based assays to stability testing.
Cell & Gene Therapy CRO Solutions
Working with a cell and gene therapy CRO across the development lifecycle fosters better integration of services and capabilities throughout your ATMP clinical trials.
Product Development and Consulting
Evidera offers a team of experts that provide end-to-end regulatory, clinical development and value and access consulting services.
Regulatory Affairs Solutions
Our staff is flexible and responsive to your needs
Managing Clinical Studies Through European Holidays
PPD® Biotech’s Samantha Hadfield, senior director of project management, Helen Dunlop, director of project management, and Rania Laguel, director of project management, provide suggestions on preparing your study for the summer holidays in Europe.