Aseptic Process Overview and Validation 2018

  • 10 Oct 2018
  • Webinar

Description

Aseptic Process Overview and Validation 2018 is a webinar dedicated to an overview of the requirements for aseptic and bulk manufacturing operations.

Aseptic Process Overview and Validation 2018 covers topics such as:

  • Facility and personnel requirements necessary to maintain microbial control
  • The difference between Aseptic and Bulk processing
  • Validation Requirements: How to Perform a Successful Media Fill
  • Basic principles of aseptic processing
  • Process Validation Requirements: Sterile Filtration Validation

Aseptic Process Overview and Validation 2018 is intended for:

  • Quality Control Departments
  • Quality Assurance Departments
  • Engineering Departments
  • Facilities Departments
  • Manufacturing Teams
  • Operations Departments
  • Quality Engineers

Past Events

Important

Please, check "Aseptic Process Overview and Validation" official website for possible changes, before making any traveling arrangements

Event Categories

Business: Facility planning & Management, Operations, Quality assurance
Health & Medicine: Medical device, Medical laboratories, Pharma

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