Auditing for Microbiological Aspects of Pharmaceutical and Biopharmaceutical Manufacturing

This 60-minute webinar will show how you can design a robust microbiological audit program for pharmaceutical and biopharmaceutical product manufacturing, that effectively assesses your facility and that of your supplier to ensure your facilities and products are free from microbial contamination.

Why Should You Attend:

The risk of non-compliance related to microbiological causes is too great, in terms of fines, potential law suits, loss of consumer confidence, and ultimately, the bottom line. This means that biopharmaceutical manufacturers must prove that their facilities and products are free from contamination.

Who Will Benefit:

This training webinar has been designed for the following personnel in pharmaceutical, biopharmaceutical and medical device companies:

Quality assurance personnel

Quality control personnel

Microbiology professionals

Validation

Manufacturing

Quality system auditors

Instructor Profile:

Henry Urbach is a founder of GMP Training, Development and Consulting (GMP TDC) LLC, a New York-based consulting organization serving life sciences industries. He has over 20 years of life sciences experience having held positions of increased responsibility in training, QA, and QC microbiology.

Note:

Use coupon code NB5SQH8N and get 10% off on registration, Valid till Dec 31st 2015.

For Registration:

http://www.complianceonline.com/auditing-for-microbiological-aspects-of-pharmaceutical-and-biopharmaceutical-manufacturing-webinar-training-702634-prdw?channel=sciencedz