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What are the principles of HEPA filtration?


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Who should attend?

Validation Engineering Maintenance

Details

Overview:
The webinar provides valuable information on differential pressure,
air velocity , flow rates, and air pressure balancing. Temperature
and relative humidity controls and specifications are also detailed.

Why should you Attend:
It is important that a clean room's HVAC system is fully understood,
properly designed and properly validated. If this is accomplished, it
will provide the environmental control necessary to meet the
regulatory particulate and microorganism levels necessary to
manufacture quality pharmaceutical product.

Areas Covered in the Session:
GMP Compliance of Clean Room Environment
Regulatory Clean Room Classification and Requirements
HVAC System Components
Clean Room Design and Layout

Who Will Benefit:
Quality Assurance
Environmental Monitoring
Microbiology
Manufacturing

Speaker Profile:
Roger Cowan is the founder and owner of R Cowan Consulting
Services LLC, a consulting company specializing primarily in the
area of pharmaceutical contract manufacturing. He has 37 years
experience in pharmaceutical quality assurance and manufacturing.
In his career, Roger has held various manager / director positions
in Quality Assurance, QC Laboratory, Technical Services Validation,
Manufacturing, and Clinical Supply manufacturing and distribution.

Event Fee: One Dial-in One Attendee Price: US$150.00

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support@compliance4All.com

http://www.compliance4all.com/control/w_product/~product_id=501928LIVE?channel=pharmiweb_Jun_2018_SEO

Prices

One Dial-in One Attendee Price: $150.00

Contact

Event Manager
support@compliance4all.com

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