SP 9th Cleanroom Seminar 2005: Definition of Cleanroom Technology Scope of Works,
Maintenance, Performance Testing and Monitoring of Cleanrooms
Date: 17th Sept 2005, Saturday
Time : 9.00 pm to 12.30 pm
Venue : Furama Riverfront Singapore Venus II & III Level 3
Address : 405 Havelock Road Singapore 169633
Tel: 6772-1567 Fax: 672-1975
Contact person : Mr V.K Pawa
Email: vinod@sp.edu.sg
Closing Date: 14 September 2005
Registration Fee:
Members of ASHRAE/SP Staff : S$80.00
Other participants : S$100.00
Full Time Students : S$20.00
Full Time Students (No lunch) : S$5.00
Payment ( Cheque Only)
Fee will cover refreshments and a buffet lunch. Payment is requested with registration.
All cheques should be made payable to “ ASHRAE Singapore Chapter “ and
mailed with your registration form to
Singapore Polytechnic
School of Mechanical and
Manufacturing Engineering
500 Dover Road
Singapore 139651
Attention: Mr V. K Pawa
PDU ( Professional Engineers Board)
3 PDUs were awarded for the 8th seminar.
3 CE units for NEBB(USA) were awarded
for the 8th seminar.
Synopses of Presentations
Definition of Cleanroom Technology Scope of Works in Consideration of The Interfaces
Involved.
The profitability and functionality of a cleanroom are dependant upon the following:
* up-to-date technical planning
* execution of the work.
Particularly important for the execution is the way in which individual packages and areas of
performance of the chosen companies are combined. The presentation will demonstrate how the
scope of works is to be put together and clarify areas of responsibility. A special focus here is the
problems surrounding the interfacing of individual packages.
Is Cleanroom Cleaning Necessary?
* Cleanroom Danger
* The Human Factor
Particulates are deposited directly onto surfaces such as floors, walls, work
surfaces, and machinery. They may not affect products at the time they are
deposited, but over time they pose an increasing threat to your products by causing physical disturbance
and eventual breakdown. Cross-contamination is the most significant cause of downtime
and loss of yield within a cleanroom environment. Pharmaceuticals, Manufacturing.
Performance Testing and Certification of Semi-conductor and Pharmaceutical cleanrooms.
This presentation will cover:
* Federal Standard 209E
* ISO 14644-1 and ISO 14644-2 standards
* Scope/limitations of some of the references
* Choice of tests
* Discussion on some tests and analytical methods
* Certification reports
Monitoring Cleanrooms
The following will be discussed in this paper:
· Why monitoring is important.
· What needs to be monitored:
* Particles
* ESD
* TRH
· Cleanroom differential Pressure
· Where to monitor .
· Standard tools used for monitoring.
For more information
Download registration form & programme details