Europe
HDR UK will release seven new health data hubs, providing over 100 doctors, scientists, and researchers with the medical histories of millions of NHS patients. They aim to aid research for new medicines, treatments, and technologies across the country, HDR’s...
Uncategorized
What Is It? ISO 13485 is a quality management system that is used internationally. It controls safety in work environments, risk management, and design, and creates requirements for inspections, documents, procedures, and verification of safety and effectiveness of...
North America
This article was updated June 2, 2025. The FDA finalized guidance in 2019 regarding placebos and blinding. FDA’s Guidance on Placebos:A placebo is an inactive substance or procedure used in clinical trials to determine whether participant responses result from...
China
Overview of China’s National Medical Products Administration (formerly CFDA), their reform, medical device registration, drug registration, …
Europe
This article was updated June 2, 2025. Medical devices in Italy are subject to the same regulations as all countries in the European Union (EU), which were implemented in 2017. Here, you can find out more information on the EU MDR and IVDR regulation. However, there...
