How to Develop PAT Approach-Regulatory Compliance 2015

  • 18 Jun 2015
  • Webinar

Description

How to Develop PAT Approach-Regulatory Compliance 2015 is a webinar that covers topics such as:

  • Regulatory impact of implementing PAT approach in R&D and production
  • The fundamental concepts behind the FDA PAT initiative
  • Efficient on-line and at-line tools for predicting quality attributes based on process data
  • Use of multivariate data analysis (MVDA) and statistical process control
  • Tools for root cause determination, trending analysis and visualization
  • Design space verification and real time quality assurance

How to Develop PAT Approach-Regulatory Compliance 2015 is intended for:

  • Process engineers
  • Formulators
  • Quality assurance personnel
  • Validation specialists
  • Anyone involved in risk mitigation and regulatory compliance
  • Production managers

Past Events

Important

Please, check "How to Develop PAT Approach-Regulatory Compliance" official website for possible changes, before making any traveling arrangements

Event Categories

Health & Medicine: Medical device, Pharma
Science: Life Sciences & Biology

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