US FDA and PATH-MVI collaborate

12 October 2008

The US Food and Drug Administration has announced a collaboration with the PATH Malaria Vaccine Initiative to develop laboratory tests to better predict the level of safety and effectiveness of experimental malaria vaccines before they are used in human clinical trials.

"This collaboration with the PATH-MVI supports the overall mission of the FDA and specifically the agency's work under our Critical Path Initiative," said Jesse Goodman, Director of the FDA's Center for Biologics Evaluation and Research, adding: "we are actively seeking ways to help organizations such as PATH develop safe and effective products that can benefit the public health both in the USA and globally."

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