Patient Registries: An Underused Resource for Medicines Evaluation
Published 1 January 2020 Patient registries, ‘organised systems that use observational methods to collect uniform data on a population defined by a particular disease, condition, or exposure, and that is followed over time’, are potentially valuable sources of data for supporting regulatory decision-making, especially for products to treat rare diseases. Nevertheless, patient registries are greatl
https://www.lupop.lu.se/article/patient-registries-underused-resource-medicines-evaluation - 2025-04-11