Why is FDA at my facility, and what do I do during an inspection? 2016

  • 21-22 Jul 2016
  • Cape Town, South Africa

Description

Why is FDA at my facility, and what do I do during an inspection? 2016 is a seminar that covers topics such as:

  • Step by step instructions to handle FDA inspections
  • Which FDA sanctions apply to you, and how to operate in compliance with FDA requirements
  • What is a front room and back room? Do you need one?
  • How to handle day by day inspection scenarios?
  • Are your SME’s the right people?
  • Runners and Scribes? What do they do?
  • Steps for responding to 483’s and Warning Letters
  • Why responses to 483’s and Warning Letters are critical?

Why is FDA at my facility, and what do I do during an inspection? 2016 brings together:

  • Subject Matter Experts (SME)
  • Top and Middle Management
  • Compliance Management
  • Quality Assurance/management
  • Laboratory
  • Manufacturing
  • Regulatory Personnel

Past Events

Important

Please, check "Why is FDA at my facility, and what do I do during an inspection?" official website for possible changes, before making any traveling arrangements

Event Categories

Business: Internal Audit & Compliance, Quality assurance
Government & Global Issues: Law & Regulations
Health & Medicine: Healthcare, Medical device, Medical technology, Pharma
Industry: Beauty & Natural products, Food & Beverages
Science: Life Sciences & Biology

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