Clean Room Technology
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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:
• Design Engineers
• Contractors
• Equipment Manufacturers
• QA/QC
• Regulatory Affairs
• Production
• Maintenance
Description
This 2-day 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.
Other Courses of Interest
Critical Process Cleaning and Cleaning Validation
Feb 27 2012, Amsterdam, The Netherlands
Critical Process Cleaning and Cleaning Validation
Mar 26 2012, New Brunswick, NJ
Current Good Tissue Practices (cGTPs)
Design Control and Product Validation
Mar 12 2012, Amsterdam, The Netherlands
Endotoxin Testing: Drugs, Medical Devices and Biopharmaceuticals
Environmental Control and Monitoring
Microbiological Control and Validation
Apr 16 2012, Burlingame, CA
Risk Management Today: Complying with the ISO 14971: 2007 Standard
Sterile Products: Formulation, Manufacture and Quality Assurance
Jun 12 2012, Burlingame, CA
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