Regulatory Requirements and Principles for Cleaning Validation 2019

  • 2019
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Description

Topics
  • The FDA perspectives on cleaning validation and areas of concern during regulatory inspections
  • The importance and underlying principles of cleaning validation and the requirements to have adequate cleaning procedures for manufacturing equipment in contact with the product
  • How to prepare and defend your own cleaning validation approach/program and avoid costly delays and/or rejections by regulatory agencies
  • Cleaning validation procedures, protocols and reports that meet current FDA, WHO, PIC/S and EU regulations
Who should Attend
  • Quality professionals
  • Senior quality managers
  • Validation engineers
  • Production supervisors
  • Quality engineers
  • Process owners
  • Quality auditors

Past Events

Important

Please, check "Regulatory Requirements and Principles for Cleaning Validation" official website for possible changes, before making any traveling arrangements

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Business: Quality assurance
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Health & Medicine: Healthcare, Medical device, Medical laboratories, Pharma
Technology: Biotechnology

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