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CfPA - The Center for Professional Advancement, 90 Minute Accredited Online Training
January 14, 2014 at 11:00 a.m.–12:30 p.m. (ET)
Who Should Attend
This online training will benefit professionals in the Biopharmaceutical, Vaccine, Cellular/Gene/Tissue Therapy, and other Biological Products Industries, and—because of the many common concerns—the traditional pharmaceutical industries as well. Auditors, Managers, Supervisors, Scientists, Technicians, and other professionals in Quality Assurance, Quality Control, Regulatory Affairs, Stability Testing, Production, and Engineering will benefit as will any person whose job includes planning, executing, reviewing and approving stability protocols, reports, and programs. Description
This course will be available On Demand: January 15, 2014
This intensive 90-minute accredited online training course focuses on becoming proficient at reviewing and auditing stability Protocols, Reports, and Programs. The overall approach is to turn theory into practice so you can put what you learn in this course to immediate use to assure your company’s stability activities, and those of any contract facilities, meet the regulatory and technical requirements and expectations of US FDA and EU EMA authorities. The course materials include comprehensive checklists to facilitate your protocol reviews, report reviews, and program 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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Tom Pritchett, Ph.D.
Thomas J Pritchett, Ph.D., has worked with US, European, and Canadian pharmaceutical, biopharmaceutical, and biologics industries for more than 25 years, during which he has gained considerable experience in regulatory and technical aspects of Quality Assurance, Quality Control and CGMP Compliance for both investigational and marketed products. He is also an experienced teacher, and has been directing courses for the Center for Professional Advancement since 1995. In addition, Dr. Pritchett has provided training sessions for the US FDA and for regulators and industry professionals in the Gulf Cooperation Council (GCC). Dr. Pritchett is also an active industry consultant and the co-founder/publisher of the newsletter BioQuality (www.bioquality.biz).
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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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