October 2016: the dangers of a quicker authorisation process for drugs episode artwork

EPISODE · Oct 21, 2016 · 9 MIN

October 2016: the dangers of a quicker authorisation process for drugs

from DTB Podcast · host BMJ Group

Why should we worry about the new European Medicines Agency (EMA) pilot project to accelerate the approval of new drugs? James Cave (DTB Editor-in-Chief) and David Phizackerley (DTB Deputy Editor) discuss the October issue Editorial, that looks at the pros and cons of this new trend both in the USA and Europe. Read the full article here: http://dtb.bmj.com/content/54/10/109.full. Also in this podcast: • the use of the new antibiotic Fosfomycin trometamol for the treatment of acute uncomplicated lower urinary tract infections (UTIs) –http://dtb.bmj.com/content/54/10/114.abstract; • as well as the "health condition" of point-of-care tests for respiratory tract infections (RTI) in improving diagnosis capabilities in GP surgeries - http://dtb.bmj.com/content/54/10/117.full.

Episode metadata supplied by the publisher feed · Published Oct 21, 2016

Embed this episode

NOW PLAYING

October 2016: the dangers of a quicker authorisation process for drugs

0:00 9:16

No transcript for this episode yet

We transcribe on demand. Request one and we'll notify you when it's ready — usually under 10 minutes.

No similar episodes found.

No similar podcasts found.

Frequently Asked Questions

How long is this episode of DTB Podcast?

This episode is 9 minutes long.

When was this DTB Podcast episode published?

This episode was published on October 21, 2016.

Can I download this DTB Podcast episode?

Yes. Use the download control on the episode player to save the publisher-provided media file.
URL copied to clipboard!