Environmental Monitoring (EM) Program Basics

This training program on applicable regulations pertaining to clean room environmental monitoring (EM) programs will discuss the basics of setting a robust and effective EM program.

Why Should You Attend:

This 90-minute webinar will discuss various broad and critical aspects of an effective EM program such as the phases of a cleanroom EM program–pre-monitoring of a cleanroom prior to facility validation, implementation of routine EM using facility validation data and post-validation.

Who Will Benefit:

This webinar will provide a great resource to product manufacturers with personnel in the pharmaceutical, biotechnology, biologics, drugs, diagnostics, cell therapy, and medical device industries.

Quality Control

Quality Assurance

Microbiologists, Facilities

Chemists, Analysts

Manufacturing

Validation

Facilities

Materials Management

Instructor Profile:

Upon earning a degree in Zoology at North Carolina State University, Joy McElroy 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. In 1998, Ms. McElroy moved to Wyeth Lederle and worked in quality assurance, performing GMP compliance audits, batch record reviews, and holding annual GMP training for new employees.

Note:

Use coupon code NB5SQH8N and get 10% off on registration, Valid till Dec 31st 2016.

For Registration:

http://www.complianceonline.com/environmental-monitoring-em-program-basics-webinar-training-704377-prdw?channel=sciencedz