New FDA Expectations for Endotoxin Testing
New FDA guidance documents changes the requirements for bacterial endotoxin testing of medical devices. This webinar will cover the four key points that need to be addressed when submitting a (510(k)). Information will also be presented on the test methods, endotoxin limits, and sampling plans.
Duration: | 15-minutes |
Dates and locations: | Available On Demand - October 6, 2017 |
Website: | https://event.on24.com/wcc/r/1532208/F8986CFF77BCB... |
Hosted by: |
Espergaerde, Denmark
Aa. Louis-Hansens Alle 11
Espergaerde
3060
Denmark
T +45 (0) 49 12 79 72
Itasca, Illinois, USA
1500 W. Thorndale Ave
Itasca, IL
60143
United States
T (630) 285-9121
Mexico City, Mexico
James Watt No. 22
Cuautitlan Izacalli
Mexico
CP 54730
Mexico
T + 52 (55) 2620 9076
Nelson Labs Europe – Leuven, Belgium
Romeinsestraat 12
Leuven
3001
Belgium
T +32 (0) 16 40 04 84
Nelson Labs Fairfield, New Jersey, USA
122 Fairfield Road
Fairfield, NJ
07004-2405
United States
T (973) 227-6882
Ontario, California, USA
687 S. Wanamaker Avenue
Ontario, CA
91761
United States
T (909) 969-2302