Environmental Monitoring Program at FDA Regulations - 2017

MessageThis Webinar is over
Date Aug 10, 2017
Time 10:00 AM
Cost 150.00
Online
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, 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: +1-800-447-9407
Email: support@compliance4All.com

 


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