Search Recorded Webinars:
GlobalCompliancePanel
GlobalCompliancePanel
Featured Speakers
Anthony DeMarinis Anthony DeMarinis
Quality Systems Manager,
Sealed Air

Honorio Silva Honorio Silva
Vice-President,
Inter American Foundation for Clinical Research Director, Pan American Federation of Associations of Medical Schools Caracas, Venezuela

Peter C. Teuten Peter C. Teuten
President and Chief Risk Architect,
Teuten Risk Consulting
Partial Client List
Customer Testimonials
Nice response to my questions and good suggestions for moving forward.

Some of these sessions are too basic - this one had a good mix of basic and details. The tips are helpful. One comment: a little more discussion regarding the use of Detection in FMEAs would be useful since many do not advocate its use. Thanks,

I especially liked that the Q&A session after the webinar was long enough to not only address my own questions but also to learn from the questions from the other participants in the webinar.

Very thorough understanding of the history/progression of the guidances, and very helpful evaluation of current and potential directions. Excellent presentation skills, very engaging.

Like
8 People like this

Call: 800-447-9407

Fax: 302-288-6884

July 16th & 17th, 2015
San Diego, CA

Casper Uldriks
Tougher Import Rules for FDA Imports in 2015

FDA's and the Customs and Border Patrol Service (CBP) have become increasingly sophisticated and equally demanding in the submission of information and adherence to government procedures.

Registration

July 30 & 31, 2015
Philadelphia, PA

Dan O'Leary
Statistical Techniques for Medical Device Manufacturers

The FDA's Quality System Regulation (QSR) requires device manufacturers to identify valid statistical techniques to "establish, control, and verify the acceptability of process capability and product characteristics."

Registration

August 6th & 7th, 2015
SFO, CA

John Zorich
The Statistics of: Design Verification, Process Validation, and Statistical Process Control

This 2-day seminar provides a 1-day introduction to the statistical tools used to analyze Design Verification data and Process Validation results. The 2nd day is spent on Statistical Process Control and Process Capability Indices.

Registration

October 22nd & 23rd, 2015
Los Angeles, CA

David R. Dills
Complaint-Handling, MDR and Recall Management

An effective complaint handling system is an extremely important part of any quality system. Manufacturers should understand that any complaint received on a product shall be evaluated and, if necessary, thoroughly investigated and analyzed, and corrective action shall be taken.

Registration

More
Customer Testimonials
Nice response to my questions and good suggestions for moving forward.

Todd Rist

Simplexity



Some of these sessions are too basic - this one had a good mix of basic and details. The tips are helpful. One comment: a little more discussion regarding the use of Detection in FMEAs would be useful since many do not advocate its use. Thanks,

Lance Mason

Smiths Medical



I especially liked that the Q&A session after the webinar was long enough to not only address my own questions but also to learn from the questions from the other participants in the webinar.

Dania P

Next Breath



Very thorough understanding of the history/progression of the guidances, and very helpful evaluation of current and potential directions. Excellent presentation skills, very engaging.

Karen Wesley

Dendreon



Copyright © 2015 GlobalCompliancePanel. All rights reserved. Netzealous