Wednesday, May 14, 2008

FDA COMPLIANCE SOLUTIONS EVENTS

May:

Introduction to Computer Validation, Bosnijek,SarajevoBosnia,

May 5-6, Philip E. Sax, Director

 

June:

GLP Seminar, Millipore,Billerica,Mass.

June 6-7, Dr. Ken Clever, Director, Philip E. Sax, Lecturer

Validation of Computer Systems, R&D,
Center for Professional Advancement
www.cfpa.com

June 13-15, New Brunswick, New Jersey,
Philip E. Sax, Director

Using Risk Assessment as a Planning Tool for Validation,
Institute of Validation Technology,Philadelphia ,
www.IVThome.com

June 16, Philip E. Sax, Presenter

Compliant Internet and Open Source Software Systems,
Network Infrastructure and Computer System Validation; Barnett International
www.barnettinternational.com

June 30, Philadelphia Pa, Philip E. Sax, Presenter

Impact of new FDA "Guidance for the Content of Premarket Submissions for Software Contained in Medical Devices",
Barnett International Web Conference www.barnettinternational.com

June 20 , Philip E. Sax, Presenter

 

July:

When to Revalidate,
San Juan, Puerto Rico,
Institute of Validation Technology
www.IVTHome.com

July 13, Philip E. Sax. Presenter

Coordination of validation Programs and Projects in a Multidisciplinary Environment,
San Juan, Puerto Rico, Institute of ValidationTechnology,

July 14, Philip E. Sax, Presenter

 

August

Validation of Computer Systems, Manufacturing,
Center for Professional Advancement,
www.cfpa.com

August 8-10,New Brunswick, New Jersey,
Philip E. Sax, Director

Good Laboratory Practice,
Center for Professional Advancement
www.cfpa.com

August 17-19, New Brunswick,NJ, Dr. Shib Mookherja, Director, Philip E. Sax, Lecturer

 

September

Using Risk Assessment as an Infrastructure  Planning Tool ,
Annual IT Infrastructure Qualification Summit, Pharma IQ,

Philip E. Sax, Present
September

 

October 

Good Laboratory Practice,
Center for Professional Advancement,
www.cfpa.com

October 10-12, Amsterdam, TheNetherlands,
Dr. David Ford,
Director,Philip E. Sax