2018 - What are the principles of HEPA filtration?

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-AT-compliance4All.com