THIS RAW MATERIALS RISK MANAGEMENT TRAINING COVERS 2015 - Microbiological Risk: Do I Really Need to Test Raw Materials for Microorganisms
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Category Biotech;
Deadline: January 20, 2015 | Date: January 20, 2015
Venue/Country: Palo Alto, U.S.A
Updated: 2015-01-05 21:40:49 (GMT+9)
Call For Papers - CFP
This webinar will cover the regulatory perspective in testing raw materials for microorganisms and how you can manage the risk of raw materials being the major source of microbial contamination in your medical product manufacturing process. Why Should You Attend:Raw materials are often the major source of microbial contamination that is introduced into the manufacturing process. Raw materials of natural origin, such as animal and plant source, support an extensive and varied microflora. Some of these pose a risk to the product and patient.Who Will Benefit:This training webinar has been designed for the following personnel in pharmaceutical, biopharmaceutical and food manufacturing companies:Quality assurance personnelQuality control personnelMicrobiology professionalsRegulatory and compliance managementInstructor Profile:Henry Urbach, is the founder of GMP Training, Development and Consulting, GMP TDC LLC, a New York-based consulting organization serving the life sciences industries. He has over 20 years of life sciences experience having held positions of increased responsibility in GMP training and QC microbiology.
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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