GMP Tips - caPA and Design Control - July 28, 2008

Recently three companies manufacturing medical devices received Warning Letters from the FDA. A large focus was on caPA (Corrective and Preventive Action) and Design Control.

One way to remain "current" with the GMP and QSR regulations is to read Warning Letters issued by FDA. Read these three Warning Letters.

Go to: www.gmptrainingsystems.com/asp/resources.asp
Click on Timely Resource Articles and scroll down.

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New for 2008! Two new Survival Kits

• Survival Kit for Regulatory Inspections
• Validation Survival Kit
• Statistics Survival Kit coming soon
  

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Fundamentals of GMP/QSR Oct 8 - 9 Anaheim, CA

Fundamentals of GLP Oct 8 Anaheim, CA
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Fundamentos de las Regulaciones de Buenas Practicas de Manufactura y Sistemas de Calidad
Oct 22 - 23 Mexico City, Mexico
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