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Failure to establish and maintain procedures for implementing corrective and preventive actions is commonly cited in FDA 483s and warning letters. CTG can help you identify best practices to achieve your CAPA and adverse event goals through services that include:
  • Joint technology selection and vendor audit services for CAPA and adverse event reporting systems
  • Process improvement for CAPA and adverse event reports business processes
  • CAPA and adverse event reporting best practices training

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