Sterile Filtration of Pharmaceutical Products – Validation and Regulatory Requirements 2019

  • 04 Apr 2019
  • Webinar

Description

Sterile Filtration of Pharmaceutical Products Validation and Regulatory Requirements 2019 is a webinar that covers topics such as:

  • Sterility assurance of sterile filtration
  • Sterile filtration—importance of quality
  • Discussion of different filtration media properties and retention mechanisms
  • Sterile filtration system design
  • Validation of sterile filter systems
  • Methods for sterilization of filters
  • Integrity testing
  • Microbial retention challenge testing
  • Extractable/leachable testing
  • Product compatibility testing
  • FDA/EU GMP regulatory requirements

Sterile Filtration of Pharmaceutical Products Validation and Regulatory Requirements 2019 is intended for:

  • Environmental Monitoring Departments
  • Quality Assurance Departments
  • Manufacturing Departments
  • Microbiology Departments
  • Engineering Departments
  • Validation Departments
  • Maintenance Departments

Past Events

Important

Please, check "Sterile Filtration of Pharmaceutical Products – Validation and Regulatory Requirements" official website for possible changes, before making any traveling arrangements

Event Categories

Business: Quality assurance
Health & Medicine: Pharma
Science: Engineering

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