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CfPA-The Center for Professional Advancement, Online Live
December 13, 2018 at 11:00 a.m.–12:30 p.m. (ET)
Who Should Attend?
This training will benefit professionals in the pharmaceutical, medical device, biotechnology, cosmetic and food industries as well as those in FDA regulated industries. It will be especially valuable to professionals in Quality Assurance, Engineering, Validation and Manufacturing. Directors, Managers, Technical writers and General staff charged with the responsibility for creating, reviewing, approving and implementing written standard operating procedures and instructions will find this course highly beneficial as well. Course Description
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Organized by:
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CfPA-The Center for Professional Advancement |
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Invited Speakers:
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 Joy McElroy, Consultant to the pharmaceutical and biotech industries |
With 10 years of experience as a consultant, and over 20 years total experience in the pharmaceutical and biotech industries, Ms. McElroy has gained extensive knowledge of Quality Assurance, Process and Cleaning Validation, and Equipment Qualification. She has written and executed Equipment Qualification and Validation Protocols for numerous Companies. Ms. McElroy specializes in Equipment Qualification, Sterilization, Cleaning Validation, and GMP Compliance Auditing. In 2013 Ms. McElroy started her own company, Maynard Consulting Company, which provides top engineers, auditors, and validation specialist to pharmaceutical, biotech and medical device clients worldwide.
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Deadline for Abstracts:
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n/a
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Registration:
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Please click here for registration information.
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E-mail:
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Jmorbit@cfpa.com
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Can't Make this LIVE Webinar?
Simply select the On Demand option when registering and we will send you the link to view the recorded version.
This course will be available On Demand: December 14, 2018