ResearchBib Share Your Research, Maximize Your Social Impacts
Sign for Notice Everyday Sign up >> Login

Online Training 2017 - Environmental Monitoring – Knowing your cleanroom

Date2017-05-11

Deadline:2017-05-11

VenueNew Hyde Park, USA - United States USA - United States

Keywords: Environmental Monitoring; FDA and ISO regulations; Clean room

Websitehttp://bit.ly/2ojhvfQ

Topics/Call fo Papers

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:
http://bit.ly/2ojhvfQ
Email: referrals-AT-complianceglobal.us
Toll Free: +1-844-746-4244
Tel: +1-516-900-5515
Fax: +1-516-900-5510

Last modified: 2017-04-18 19:56:34