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HUM-MOLGEN
-> Events
-> Courses and Workshops |
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April 18, 2017 |
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Compliance4All, Online
2017-06-07
Overview:
Successful autoclave Performance Qualification starts with a fundamental
understanding of steam sterilization microbiology.
Why should you Attend:
Sterilization process parameters will be laid out as a basis for conducting
autoclave performance qualification studies. Whether qualifying a new
autoclave installation orcontinuing maintenance of existing equipment, there
are specific expectations for steam sterilization that must be met.
Areas Covered in the Session:
Autoclave Performance Qualification expectations
Regulatory and GMP requirements for steam sterilization
Validation tools for use in an autoclave
Common questions, problems and cGMPs
Who Will Benefit:
Quality Assurance Managers
Supervisors
Validation personnel
Sterility Assurance personnel
Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support@compliance4All.com
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Organized by:
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Compliance4All |
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Invited Speakers:
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Speaker Profile:
Danielle DeLucy MS, is owner of ASA Training and Consulting, LLC which
provides Pharmaceutical and Biologics based companies with training and
quality systems assistance in order to meet Regulatory compliance.
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Deadline for Abstracts:
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2017-06-06
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Registration:
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Full Details & Registration Link: http://www.compliance4all.com/control/w_product/~product_id=501334LIVE?channel=hum-molgen_Jun_2017_SEO
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E-mail:
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support@compliance4All.com
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