Late Phase
ICON’s Lifecycle Sciences group is dedicated to designing and implementing Phase IV and pre-approval solutions.
Services
ICON’s services include:
Phase IV Clinical Trials
ICON’s Lifecycle Sciences group is uniquely positioned to provide strategic guidance and a comprehensive yet flexible approach to maximise the benefit of these programs.
Patient Registry (Disease or Product)
A Patient Registry is an observational study enrolling individuals with a common characteristic, e.g. disease or treatment, and collecting data for varying time periods, frequently several years. The registry data are used to address questions regarding patient outcomes over time as they receive the standard of care from their healthcare provider.
Pregnancy Registries
Similar to a Patient Registry, a Pregnancy Registry observes what happens over time in normal medical practice, but focuses on outcomes data from patients exposed to a product while pregnant.
Similar to a Patient Registry, a Pregnancy Registry observes what happens over time in normal medical practice, but focuses on outcomes data from patients exposed to a product while pregnant.
Safety Surveillance
Safety Surveillance Studies are designed to observe adverse drug reactions associated with a product based on real-world clinical use.
Retrospective Data Analysis
Our researchers are adept at designing and conducting insightful analyses, while understanding and addressing the limitations inherent in retrospective data sources.
Our researchers are adept at designing and conducting insightful analyses, while understanding and addressing the limitations inherent in retrospective data sources.
Development and Validation of Patient Reported Outcomes (PROs) ICON’s Lifecycle Sciences group provides a full range of customised solutions for all PRO research design needs, from providing strategic recommendations for appropriate PRO measures to developing, testing, and validating an original questionnaire.