Knowledge Center > Education > Webinars

Webinars

Ready for a webinar?

Build your testing knowledge with our webinar series. Our engaging presenters will guide you through timely, relevant testing topics that challenge you to become a thought leader for your company. Learn about upcoming webinars.
 

Next Webinar:

TBD

Previous Webinars:
 

Download: EO Sterilization- Batch Release for Small or Infrequent Lots slide deck
Download: Particulates: Their Role in the Medical Device Industry
Download: Packaging Test Methods for Validation of Sterile Barrier Materials
Download: Masks, Gowns & Drapes- Testing the Barrier Performance of Your Product
Download: Radiation Sterilization Validations
Download: Ethylene Oxide Sterilization
Download: How to tell if my device is really clean
Download: The Big Three: Cytotoxicity, Sensitization & Irritation
Download: Cleaning Validations of Reusable Medical Devices
Download: Tissue Process Validation Concepts 

This was easily the best webinar I’ve attended in years. Most are merely infomercials for a vendor/service provider, and frankly, are quite boring. This webinar was not only engaging, but loaded with information, clearly and professionally presented. My compliments.
- Marc, Director of R&D, Medical Device Manufacturer
 
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Upcoming Webinars

This webinar is designed to provide information for the beginner and the intermediate level person seeking further details into performing cleaning validations of reusable medical devices.

Location:
February 24, 2011
1:00 p.m. EST (12:00 p.m. CST, 11:00 a.m. MST, 10:00 a.m. PST)

Date: 2/24/2011 11:00:00 AM

The purpose of this webinar will be to provide quality assurance, design engineers, project engineers and all medical device manufacturers the knowledge to make decisions regarding which tests should be used to validate their sterile barrier system. 

Location:
March 30, 2011
1:00 p.m. EST (12:00 p.m. CST, 11:00 a.m. MST, 10:00 a.m. PST) 

Date: 3/30/2011 11:00:00 AM

This webinar is aimed toward companies that develop such products or manufacture other cardiovascular medical devices or devices that are likely to come in contact with a patient’s bloodstream.

Location: June 29, 2011
1:00 p.m. EST (= 12:00 p.m. CST, 11:00 a.m. MST, 10:00 a.m. PST) 
Date: 6/29/2011 11:00:00 AM

How do you sterilize product when you only have enough product produced to make up one sterilization load?  How do you demonstrate a sterility assurance level (SAL) of 10-6 when you do not have the time or sample quantity required for a full EO validation? 

Location:
Date: 9/14/2011 1:00:00 PM

The intent of the webinar is to provide those who perform or review process validations with the concepts and knowledge needed to properly set up the validation and interpret the data. The webinar includes concepts which are also addressed in the upcoming Microbiological Surveillance document from AATB. Q&A time will be provided at the end of the webinar.

Location:  
 Webinar is scheduled for 11:00 am MST (which is 1:00 pm EST, 12:00 pm CST, 10:00 am PST)

Date: 11/30/2011 11:00:00 AM

“I am always very pleased with the service provided by Nelson Laboratories. I highly recommend them. Great customer service and prompt reporting results are very helpful to my RA/QA job function.”

Barbara , RA/QA , Medical Device Manufacturer
MN:BARRACUDA