What are the principles of HEPA filtration?

Website http://www.compliance4all.com/control/w_product/~product_id=501928LIVE?channel=ourglocal_Jun_2018_SE | Edit Freely

Category Pharmaceutical Clean Rooms, HVAC system, clean patient room, clean classification room, design clean room, clean room specifications, pharmaceutical clean room class, GMP clean room

Deadline: June 10, 2018 | Date: June 12, 2018

Venue/Country: Online, U.S.A

Updated: 2018-04-18 15:34:54 (GMT+9)

Call For Papers - CFP

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: supportcompliance4All.com