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GlobalCompliancePanel
GlobalCompliancePanel
Featured Speakers
David N. Muchemu David N. Muchemu
Founder and CEO,
Quality systems International, (QSi) LLC

Steven S Kuwahara Steven S Kuwahara
Founder & Principal,
GXP Biotechnology, LLC

Janet Gough Janet Gough
Director,
GXP Documentation
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.

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7 People like this

Call: 800-447-9407

Fax: 302-288-6884

March 12th & 13th, 2015
Philadelphia, PA

Dr. Teri C Soli
Pharmaceutical Water Systems: The A to Z's of Microbial Control, Monitoring and validation

This course is designed to provide a microbiology-focused education about all aspects of water systems and how biofilm manages to thrive there.

Registration

March 19th & 20th, 2015
San Diego

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

March 19th & 20th, 2015
Washington DC

Steven Walfish
Using Statistical Methods for ICH Guidelines

This hands-on course will provide attendees with an understanding of how to apply statistical methods to the ICH Q series guidelines. The course will deliver tools, templates and insight that will allow participants to immediately begin implementation within their organization/firm.

Registration

April 2nd & 3rd, 2015
Seattle, WA

Jerry Dalfors
Quality System Regulations for Drugs, Devices, and Tablets and How to generate your DMF

Primary Student Objectives - General High Level Topics where we will move down to very specific discussion and details to generate a much higher comprehension for quality individuals even though during this course you will not have to take a final exam!

Registration

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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



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