4-Hour Virtual Seminar on Aseptic Processing and Validation

The 4-Hour Virtual Seminar on Aseptic Processing and Validation is a webinar that covers topics such as:

  • Facility and personnel requirements necessary to maintain microbial control
  • The difference between Aseptic and Bulk processing
  • The gowning requirements associated with different cleanroom classifications
  • Basic principles of microbiology and microorganism recovery in relation to cleanroom environmental monitoring (EM) and impact to product
  • The purpose of media fills, and elements critical to their success
  • Basic principles of aseptic processing, including:
  • Ways that they can impact/ improve site-specific EM and aseptic behavior issues
  • Behaviors that are or are not appropriate when working in controlled areas, and why

The 4-Hour Virtual Seminar on Aseptic Processing and Validation is intended for:

  • Quality Control Department Management and Staff
  • Quality Assurance Department Management and Staff
  • Records Managers
  • Operations Department Management and Staff
  • Engineering Department Management and Staff
  • Production Management and Staff
  • Facilities / Maintenance Management and Staff
  • Validation Management and Staff

Future Events

4-Hour Virtual Seminar on Aseptic Processing and Validation 2020

Important

Please, check the official conference website for possible changes, before you make any traveling arrangements

Prices are for evaluation only.

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