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CfPA-The Center for Professional Advancement, Online Live
April 12, 2017 at 11:00 a.m.–12:30 p.m. (ET)
Who Should Attend?
This course was designed for cGMP manufacturing professionals who are contemplating improving their process, traceability and FDA compliance with electronic batch records.
Applicable industry and roles include but are not limited to: - Pharmaceutical, Biologic, Medical Device, Dietary Supplement, Botanical, E-liquid/Vape, and CBD/Medical Marijuana production operations
- Production/Operations, QA, Formulation, IT
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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| Gretchen Rizor; MES Process Consultant and Quality Manager |
Gretchen Rizor studied Biology and Anthropology at UNC Chapel Hill and has 9 years of experience in Pharma/biotech in RTP, NC. She is proficient in parenteral batch record release, compliance gap analysis, deviation reports, CAPAs, QADC and QC micro testing. Ms. Rizor is currently an MES Process Consultant and Quality Manager over FDA-regulated manufacturing software design and validation and is a webinar speaker.
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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: April 13, 2017