FDA Inspections: From SOP to 483

FDA Inspections: From SOP to 483 is a webinar that covers topics such as:

  • Development and contents of an SOP for FDA inspection
  • How to prepare for an FDA inspection
  • How to behave during an inspection
  • Personnel training before inspection
  • Response to investigation findings
  • Limitations of the scope of an inspection
  • FDA guidance documents used by their inspectors

FDA Inspections: From SOP to 483 is intended for:

  • Quality Control Departments
  • Quality Assurance Departments
  • Regulatory Affairs Departments
  • Compliance Departments
  • CAPA Specialists
  • Engineering Departments
  • Consultants and Contractors
  • Management Representatives
  • Who may have direct interaction with FDA officials

Future Events

FDA Inspections: From SOP to 483 2020


Please, check the official conference website for possible changes, before you make any traveling arrangements

Prices are for evaluation only.

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