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Compliance Global Inc
2754 80th Avenue
New Hyde Park, NY 11040
(516) 900-5515

Compliance Global Inc
(516) 900-5515

Event Description

Overview:

This webinar will provide the proper methods and techniques required to maintain a clean room per FDA and ISO regulations. By the use of viable and non-viable testing, a cleanroom can be maintained. The results collected can determine the state of control the cleanroom operates on a continuous basis.

Why Should You Attend:

Personnel involved with monitoring, trending, and drawing conclusions from the testing related to environmental monitoring. Personnel who are uncertain their current environmental monitoring program is effective and/or meets current FDA and ISO regulations. Personnel who need to understand what controls are in place in order to maintain a state of control to their cleanroom(s).

Areas Covered in this Webinar:

Environmental monitoring is the process of testing cleanrooms to ensure these rooms maintain a state of control. Non-viable testing is testing done to monitor the amount of total particulates within a cleanroom. Viable testing is categorized into air and surface monitoring. The viable air monitoring can be further divided into passive monitoring and active monitoring. Cleaning agents are used to lower the amount of viables within a room and increased usage can be done during contamination events.

Learning Objectives:

The most appropriate cleaning agents and possible schedules for use of the cleaning agents
Trending methods in order to ensure the cleanroom is maintaining a state of control
How a cleanroom can be maintained to perform in accordance with ISO and FDA regulations

Who Will Benefit:

Pharmaceutical Manufacturing Companies
Contract Manufacturing Companies (CMOs)
Personnel involved with Environmental Monitoring Operations

Speaker Profile:

Carl Patterson, M.S. has completed twelve (13) plus years in the biotechnology, pharmaceutical manufacturing, and quality fields. He completed his Bachelor’s of Science in Microbiology from the University of Texas.

Also, has completed specialized certificates in biotechnology manufacturing, quality control, and quality assurance from UCSD, and has completed his Master’s of Science in Biomedical Quality Systems from SDSU. Through the years, has worked with several companies in regards to aseptic processing and environmental monitoring. He has helped to insure the expectations, related to aseptic processing and environmental monitoring, have been met.

For more detail please click on this below link:

https://complianceglobal.us/product/700519

Email: referrals@complianceglobal.us
Toll Free: +1-844-746-4244
Tel: +1-516-900-5515

Fax: +1-516-900-5510

There may be many networking opportunities at the Environmental Monitoring - Knowing your cleanroom - By Compliance Global Inc.. Find out more in the event details below.

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Event Details

Website: https://complianceglobal.us/product/700519...
Conference/Event Dates: 08/25/2016 - 08/25/2016
Conference/Event Hours: 1:30
Classification: B2B
Primary Industry: Clinical Pharmacology
Other Industries: Business, Clinical Pharmacology, Professional Healthcare, Sciences
Cost to Attend: Live Session for one participant Price: $175.00
Audience: Pharmaceutical Manufacturing Companies
Contract Manufacturing Companies (CMOs)
Personnel involved with Environmental Monitoring Operations
Show Owner:Compliance Global Inc.
Sponsorship: Yes
Sponsorship Details: Compliance Global Inc.

Booth Details

Booth Size Booth Cost   Available Amenities
No Exhibiting   Electricity: n/a
  Water: n/a
  Generator: n/a
  Marketing Vehicles Allowed: n/a
Other Booth Sizes Available: n/a

Advance Networking

How do I show up here?
 
Mark Travers

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