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Home > New FDA Approvals > 048 - Pfizer’s Ixifi™ (infliximab-qbtx) biosimilar receives FDA approval; Investigational device exemption approval given to first-in-kind PAD procedure; FDA launches website for sharing information for better management of antibiotic use
Podcast: New FDA Approvals
Episode:

048 - Pfizer’s Ixifi™ (infliximab-qbtx) biosimilar receives FDA approval; Investigational device exemption approval given to first-in-kind PAD procedure; FDA launches website for sharing information for better management of antibiotic use

Category: Science & Medicine
Duration: 00:12:09
Publish Date: 2017-12-14 07:00:00
Description:

December 14, 2017 

0:30 - Ixifi™ (infliximab-qbtx) receives FDA approval for all eligible indications https://www.pfizer.com/news/press-release/press-release-detail/fda_approves_new_pfizer_biosimilar 

2:37 - Investigational device exemption approval given to first-in-kind PAD proceedure

http://www.cardiovascularbusiness.com/topics/vascular-endovascular/fda-approves-trial-test-percutaneous-procedure-pad

https://www.businesswire.com/news/home/20171213005336/en/PQ-Bypass-Receives-IDE-Approval-Initiate-Study 

4:37 - FDA launches new tool for sharing information that allows doctors to better manage antibiotic use; improve patient care

https://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm588836.htm

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