When: |
10 Aug through 10 Aug 2017 | |
CFP Deadline: |
10 |
|
Where: |
Fremont, United States | |
Website URL: |
http://www.compliance4all.com/control/w_product/~product_id=501414LIVE?channel=brownwalker_Aug_2017_SEO | |
Sponsoring organization: |
Netzealous LLC DBA - Compliance4All | |
Categories: |
Education / Legal / Other - Education |
Keywords:
Event description:
Overview:
Upon completion of this training, you will be able to Describe how Clean room Environmental Monitoring Program fits into the Regulations. Explain the basis of the Four (4) Phases of Clean room transitional monitoring.
Why should you Attend:
The cost of non-compliance is therefore more than that of compliance. Are you in compliance with the FDA regulations for Cleaning Validations of your manufacturing equipment?
Areas Covered in the Session:
Applicable Regulations - Where does the EM Program fit in the Regulation? -
Role of Clean room Environmental Monitoring Program?
Basics of Setting a Robust and Effective EM Program - Key Considerations -
Relevant Material Verification Processes - Steps and Content of an EM
Program Testing Procedure
Who Will Benefit:
Quality Control,
Quality Assurance
Microbiologist, Facilities
Chemist, Analysts
Manufacturing
Speaker Profile:
Joy McElroy Upon earning a degree in Zoology at North Carolina State University, ...
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Posting date:
19 June 2017 | 142 views
Placement:
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