Course offering number:0810-204
Course ID:
23
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.
Other Courses of Interest
Critical Process Cleaning and Cleaning Validation
May 26 2010, Amsterdam, The Netherlands
Current Good Tissue Practices (cGTPs)
Design Control and Product Validation
Jul 12 2010, Amsterdam, The Netherlands
Endotoxin Testing: Drugs, Medical Devices and Biopharmaceuticals
Environmental Control and Monitoring
Microbiological Control and Validation
Risk Management Today: Complying with the ISO 14971: 2007 Standard
Sterile Products: Formulation, Manufacture and Quality Assurance
Mar 15 2010, Amsterdam, The Netherlands
Sterile Products: Formulation, Manufacture and Quality Assurance
Apr 26 2010, New Brunswick, NJ
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