Sinovac obtains production license for H1N1 vaccine in China

4 September 2009

China's State Food and Drug Administration (SFDA) has approved the registration application for PANFLU.1, Chinese biopharmaceutical firm Sinovac Biotoech's H1N1 vaccine, and has issued the company with a production license for this vaccine. Sinovac has the capacity to produce 5 million doses of vaccine before October 1, and 20 million to 30 million doses per year, said president the firm's president, Yin Weidong.

Another A/H1N1 flu vaccine, produced by Chinese pharmaceutical company Hualan Biological Engineering, is also hopeful to be given the country's second approval this week, reports the Shanghia Daily newspaper.

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









Company Spotlight



More Features in Pharmaceutical