As the trade war between the USA and China instigated by US President Donald Trump accelerates, at least the two countries’ healthcare regulators are still talking in a collaborative fashion.
Earlier this week, Xu Jinghe, Deputy Commissioner of the National Drug Administration of China (CNDA), attended the China US Exchange for Cancer Drug Development and Evaluation held jointly by CNDA and the US Food and Drug Administration.
The CNDA Center for Drug Evaluation (CDE) introduced the priority review of China's new anti-tumor drugs, and the US FDA Oncology Center of Excellence (OCE) has introduced the regulatory work of FDA in the novel anti-cancer drugs, expediting product development, listing and approving.
This article is accessible to registered users, to continue reading please register for free. A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.
Login to your accountTry before you buy
7 day trial access
Become a subscriber
Or £77 per month
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed
Chairman, Sanofi Aventis UK
Copyright © The Pharma Letter 2024 | Headless Content Management with Blaze