Clean Room Technology
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This course is available as a client site course. Please click here for more information.
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.