China manufacturing disasters highlights importance of partner due diligence, notes analyst

26 October 2018
china_credit_depositphotos_large

The recent pharma regulatory reforms by China are expected to provide opportunities for both domestic as well as foreign contract manufacturing organizations (CMOs).

However, a series of manufacturing scandals highlights the importance of performing due diligence when picking a pharma manufacturing partner in the country, says leading data and analytics company says data and analytics company GlobalData.

In July, the European Medicines Agency discovered N-nitrosodimethylamine, a probable carcinogen, in batches of the drug valsartan, which is used to treat high blood pressure and heart failure, manufactured by Zhejiang Huahai Pharmaceutical.

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 account

Become a subscriber

 

£820

Or £77 per month

Subscribe Now
  • Unfettered access to industry-leading news, commentary and analysis in pharma and biotech.
  • Updates from clinical trials, conferences, M&A, licensing, financing, regulation, patents & legal, executive appointments, commercial strategy and financial results.
  • Daily roundup of key events in pharma and biotech.
  • Monthly in-depth briefings on Boardroom appointments and M&A news.
  • Choose from a cost-effective annual package or a flexible monthly subscription
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



Today's issue

Company Spotlight





More Features in Pharmaceutical