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Course offering number:0810-204

Course ID:
23
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Clean Room Technology
9-10 October 2008
Amsterdam, The Netherlands

Who Should Attend
This course is intended for all personnel involved with the following areas of pharmaceutical and medical device sterile facilities:

  • Design
  • Construction
  • Validation
  • Operation
  • Monitoring
Other personnel who will find this course of interest include:
  • Design Engineers
  • Contractors
  • Equipment Manufacturers
  • QA/QC
  • Regulatory Affairs
  • Production
  • Maintenance

Description
This course reviews the current state of the technology associated with pharmaceutical, medical device, active pharmaceutical ingredient, medical component, R&D, and microbiological clean rooms. Regulations and guidelines for the U.S. and E.U. will be covered.

The course is conducted in an environment that encourages discussion, questions, input, and debate by the attendees. Case studies of actual rooms are presented. Attendees are invited to bring their own projects for discussion and review.




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Other Courses of Interest

Barrier/Isolater Technology for FDA Regulated Facilites

Critical Process Cleaning and Cleaning Validation
Dec 03 2008
, Dublin, Ireland

Environmental Control and Monitoring

Microbiological Control and Validation

Microbiological Quality of Water-Based Consumer Products

Sterilization Technologies and Process Validation


Related Industries

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