Showing posts with label non. Show all posts
Showing posts with label non. Show all posts

Wednesday, July 22, 2009

Rx-360 - A non-profit to help secure the supply chain (podcast)

Updated July 29, 2020

The links in the original post broke.

You might also be interested in:
Rx-360 - About Us

- - -  original post follows below  - - -

Learn about Rx-360. Listen to this Pharmaceutical Technology podcast (~ 11 mins), Podcast: A Look at Rx-360. Here's how Pharmaceutical Technology describes this podcast:

Join Angie Drakulich, Managing Editor of Pharmaceutical Technology, as she speaks with Martin Van Trieste, Vice-President of Quality for Amgen and Interim Director of Rx-360, a new nonprofit international pharmaceutical consortium, about the need for industry to come together to secure the supply chain. They will explore shared supplier audit models and FDA's take on the consortium's proposals.
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Monday, April 20, 2009

FDA GCP - Tips On Conducting non-US Studies

If you're looking to conduct clinical studies outside the U.S., you might do well to read this superb article from Bruce Mackler on GEN, "Spotlight on the FDA Outsourcing Clinicals; Medical Journal Articles; and Contract Manufacturing Liability Issues. Mackler says, "In today’s financing environment, the absence of early clinical data presents a high barrier to obtaining funding. Investors often say “show me the clinical data that show that the drug is safe and works and I will show you my money.” As a result, biopharma companies have moved into early non-U.S. clinical trials that have lower safety data burdens. These studies are being conducted in less wealthy (a.k.a., developing) countries, where Phase I trials can be more rapid and less costly. This strategy has been promoted by CROs established in these countries." The article provides some great tips, not to be overlooked. 


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