Environmental Monitoring Program at FDA Regulations - 2017
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Website http://www.compliance4all.com/control/w_product/~product_id=501414LIVE?channel=ourglocal_Aug_2017_SE |
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Category Environmental Monitoring, FDA Regulations, FDA Webinars, fda regulatory training, fda compliance training, Manufacturing, Research and Development, environmental monitoring systems, data center temperature monitoring
Deadline: August 09, 2017 | Date: August 10, 2017
Venue/Country: Online, U.S.A
Updated: 2017-06-15 15:13:16 (GMT+9)
Call For Papers - CFP
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 ProcedureWho Will Benefit:Quality Control,Quality AssuranceMicrobiologist, FacilitiesChemist, AnalystsManufacturing Speaker Profile:Joy McElroy Upon earning a degree in Zoology at North Carolina State University, Joy made her debut in the pharmaceutical industry in 1992 at Pharmacia & UpJohn performing Environmental Monitoring and Sterility Testing. Her hard work allowed her to move into a supervisory role at Abbott Laboratories where she oversaw their Quality Control Lab.Contact Detail:Compliance4All DBA NetZealous,Phone: +1-800-447-9407Email: supportcompliance4All.com
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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