Manufacturers To Record Pearl Powder Purchases For SFDA Monitoring
This article was originally published in PharmAsia News
Executive Summary
In response to a recent fake pearl powder incident, China's State FDA announced Sept. 25 that all manufacturers whose products contain pearl powder as an ingredient are required to establish records of their pearl powder purchases and a list of suppliers to make possible tracing of problematic pearl powder
You may also be interested in...
FDA’s New Dataset Aims To Assist Labs In Assessing Medical Device Biocompatibility
The US FDA’s device center has unveiled a new public dataset designed to assist chemistry laboratories in ensuring the robustness of chemical characterization methods used to assess the biocompatibility of medical devices.
Sanofi Prepares Pulmonologists As Dupixent Nears COPD Finishing Line
The French drugmaker has identified education as a key challenge ahead of its June action date for the huge-selling IL4/IL-13 inhibitor in the lung condition. An approval would make it the first biologic for the disease.
Global Pharma Guidance Tracker – March 2024
Stay up to date on regulatory guidelines from around the world with the Pink Sheet's Guidance Tracker. The complete Global Pharma Guidance Tracker, with sortable and searchable listings going back to 2014, is available online.