2017 - Environmental Monitoring Program at FDA Regulations - 2017

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-AT-compliance4All.com