Thu August 20, 2015
Auditing for Microbiological Aspects of Pharmaceutical and Biopharmaceutical Manufacturing
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at Webinar - Online
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Topic ID: 000000136-web
Start Date: Aug 20, 2015
Name of Event: Auditing for Microbiological Aspects of Pharmaceutical and Biopharmaceutical Manufacturing
Start Time: 10 AM PST | 1 PM EST
Details: This 90-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.
This webinar is designed to help organizations understand that preventing microbial contamination is the responsibility of everyone in the organization, and that everyone must play a part in it. Attendees will learn how to create a robust inspection program that includes auditing for potential sources of microbial contamination.
Areas Covered In The Session:
What do regulations say about the subject?
Sources of contamination
Preventing contamination
Controlling contamination
What about the suppliers?
Everyone has a role in contamination control
Speaker: Henry Urbach, is the founder of GMP Training, Development and Consulting (GMP TDC) LLC, a New York-based consulting organization serving Life Sciences industries. He has 20+ years of Life Sciences experience having held positions of increased responsibility in Training, QA, and QC Microbiology. His experience includes managing GMP compliance and quality systems training, implementing a training program as part of remediation, and developing an environmental monitoring training program. He is a dynamic speaker specializing in FDA and ICH compliance. He is a Certified Quality Auditor (CQA). His technical education is further complemented by his BA degree in Biology and MBA, which provide a scientific and business insight. He is a member of the ASTD, ASQ, and GMP Training and Education Association (GMP TEA).
For more details call Complystream at: (+1) 844 498 6361
show less
Start Date: Aug 20, 2015
Name of Event: Auditing for Microbiological Aspects of Pharmaceutical and Biopharmaceutical Manufacturing
Start Time: 10 AM PST | 1 PM EST
Details: This 90-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.
This webinar is designed to help organizations understand that preventing microbial contamination is the responsibility of everyone in the organization, and that everyone must play a part in it. Attendees will learn how to create a robust inspection program that includes auditing for potential sources of microbial contamination.
Areas Covered In The Session:
What do regulations say about the subject?
Sources of contamination
Preventing contamination
Controlling contamination
What about the suppliers?
Everyone has a role in contamination control
Speaker: Henry Urbach, is the founder of GMP Training, Development and Consulting (GMP TDC) LLC, a New York-based consulting organization serving Life Sciences industries. He has 20+ years of Life Sciences experience having held positions of increased responsibility in Training, QA, and QC Microbiology. His experience includes managing GMP compliance and quality systems training, implementing a training program as part of remediation, and developing an environmental monitoring training program. He is a dynamic speaker specializing in FDA and ICH compliance. He is a Certified Quality Auditor (CQA). His technical education is further complemented by his BA degree in Biology and MBA, which provide a scientific and business insight. He is a member of the ASTD, ASQ, and GMP Training and Education Association (GMP TEA).
For more details call Complystream at: (+1) 844 498 6361
Topic ID: 000000136-web
Start Date: Aug 20, 2015
Name of Event: Auditing for Microbiological Aspects of Pharmaceutical and Biopharmaceutical Manufacturing
Start Time: 10 AM PST | 1 PM EST
Details: This 90-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.
This webinar is designed to help organizations understand that preventing microbial contamination is the responsibility of everyone in the organization, and that everyone must play a part in it. Attendees will learn how to create a robust inspection program that includes auditing for potential sources of microbial contamination.
Areas Covered In The Session:
What do regulations say about the subject?
Sources of contamination
Preventing contamination
Controlling contamination
What about the suppliers?
Everyone has a role in contamination control
Speaker: Henry Urbach, is the founder of GMP Training, Development and Consulting (GMP TDC) LLC, a New York-based consulting organization serving Life Sciences industries. He has 20+ years of Life Sciences experience having held positions of increased responsibility in Training, QA, and QC Microbiology. His experience includes managing GMP compliance and quality systems training, implementing a training program as part of remediation, and developing an environmental monitoring training program. He is a dynamic speaker specializing in FDA and ICH compliance. He is a Certified Quality Auditor (CQA). His technical education is further complemented by his BA degree in Biology and MBA, which provide a scientific and business insight. He is a member of the ASTD, ASQ, and GMP Training and Education Association (GMP TEA).
For more details call Complystream at: (+1) 844 498 6361
read more
Start Date: Aug 20, 2015
Name of Event: Auditing for Microbiological Aspects of Pharmaceutical and Biopharmaceutical Manufacturing
Start Time: 10 AM PST | 1 PM EST
Details: This 90-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.
This webinar is designed to help organizations understand that preventing microbial contamination is the responsibility of everyone in the organization, and that everyone must play a part in it. Attendees will learn how to create a robust inspection program that includes auditing for potential sources of microbial contamination.
Areas Covered In The Session:
What do regulations say about the subject?
Sources of contamination
Preventing contamination
Controlling contamination
What about the suppliers?
Everyone has a role in contamination control
Speaker: Henry Urbach, is the founder of GMP Training, Development and Consulting (GMP TDC) LLC, a New York-based consulting organization serving Life Sciences industries. He has 20+ years of Life Sciences experience having held positions of increased responsibility in Training, QA, and QC Microbiology. His experience includes managing GMP compliance and quality systems training, implementing a training program as part of remediation, and developing an environmental monitoring training program. He is a dynamic speaker specializing in FDA and ICH compliance. He is a Certified Quality Auditor (CQA). His technical education is further complemented by his BA degree in Biology and MBA, which provide a scientific and business insight. He is a member of the ASTD, ASQ, and GMP Training and Education Association (GMP TEA).
For more details call Complystream at: (+1) 844 498 6361
show less
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Webinar - Online
420 Lexington Avenue Suite 300, New York City, NY 10170
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