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CfPA-The Center for Professional Advancement, 90 Minute Accredited Online Training
July 16, 2014 at 11:00 a.m.–12:30 p.m. (ET)
Who Should Attend
This practical online training will benefit professionals and associates in the Pharmaceutical, Biotechnology, Medical Device, and Cosmetics industries including Engineers, Managers and Associates in:
• QA/QC
• Quality Compliance
• Quality Audit
• Supply Chain
• Operations
• Technical Services
• Regulatory Affairs Description
This course will be available On Demand: July 17, 2014
The visibility of Supplier Qualification to regulatory agencies has increased in recent years. The complex nature of supply chain has necessitated a critical evaluation of this complex network.
This practical, accredited course will outline details of the requirements for a robust Supplier Qualification program for FDA regulated industries with focus on risk assessment techniques and quality audits.
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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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Maria Buck, Consultant to the Pharmaceutical Industry
Maria Buck has over 20 years in the Pharmaceutical Industry. During this time, Ms. Buck has held roles in Quality Assurance, Quality Engineering, Quality Compliance and R&D. She has conducted domestic and international audits of API, excipient, component, third-party packaging, logistics and finished product manufacturing facilities. She holds a B.S. in Chemistry from Northern Arizona University and has received ASQ CQA and CQA certifications.
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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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sberg@cfpa.com
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