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Medical Device Workshop on FDA Inspections, Warning Letters and CAPA
Tuesday, May 22 - Wednesday, May 23
Sheraton Crystal City, Crystal City, Va.
The percentage of CAPA system deficiencies in FDA warning letters has increased in the past five years. This conference will provide you with the tools to avoid warning letters, enable you to demonstrate your compliance initiatives and teach you how to respond to a warning letter. Learn how properly to integrate and implement your CAPA program to improve internal processes and products and better achieve business objectives. Network with a distinguished panel of experts for an in-depth examination of what CAPA is, how the concept has evolved and whether it accomplishes what industry needs and what FDA expects. Visit MTLI online for more information.
Sheraton Crystal City, Crystal City, Va.
The percentage of CAPA system deficiencies in FDA warning letters has increased in the past five years. This conference will provide you with the tools to avoid warning letters, enable you to demonstrate your compliance initiatives and teach you how to respond to a warning letter. Learn how properly to integrate and implement your CAPA program to improve internal processes and products and better achieve business objectives. Network with a distinguished panel of experts for an in-depth examination of what CAPA is, how the concept has evolved and whether it accomplishes what industry needs and what FDA expects. Visit MTLI online for more information.
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