QbD Development Process Evaluating Critical Steps 2019

  • 25 Jan 2019
  • Webinar

Description

QbD Development Process Evaluating Critical Steps 2019 is a webinar that covers topics such as:

  • Critical quality attributes (CQA) is a physical, chemical, biological, or microbiological property or characteristic that should be within an appropriate limit, range, or distribution to ensure the desired product quality
  • Quality target product profile (QTPP) forms the basis for design and the development of the product. Considerations for the Quality Target Product Profile (ICH guideline Q8 R2)
  • Risk Assessment (RA)one can recognizing critical attributes that are going to affect final quality of product
  • Process Analytical Technology (PAT) which is a Framework for Innovative Pharmaceutical Development, Manufacturing and Quality Assurance

QbD Development Process Evaluating Critical Steps 2019 is intended for:

  • Regulatory Managers, Associates
  • Regulatory Affairs Directors
  • Technical Services Mangers
  • Regulatory Compliance Directors, Manager
  • Materials Management
  • Plant Manager
  • Quality Control Director, Manager

Past Events

Important

Please, check "QbD Development Process Evaluating Critical Steps" official website for possible changes, before making any traveling arrangements

Event Categories

Business: Innovations, Internal Audit & Compliance, Quality assurance
Health & Medicine: Pharma

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