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HUM-MOLGEN
-> Events
-> Courses and Workshops |
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October 26, 2015 |
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CfPA-The Center for Professional Advancement, Burlingame, CA
April 4, 2016
Who Should Attend? This intensive one day course will benefit anyone involved in the pharmaceutical and medical device industries. It will be especially valuable to professionals involved in:
• Quality Control • Quality Assurance • Production • Validation • Engineering • Audit • Documentation • Training • Technical Support • Maintenance • Development 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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William G. Marshall; President, William G. Marshall & Associates |
William G. Marshall is President of William G. Marshall and Associates. He has nearly forty years experience in the Pharmaceutical and Medical Device Manufacturing Environment. Mr. Marshall has held Director level and Chief Operating Officer positions with large multinational pharmaceutical corporations as well as start-up ventures. He has been the Director of a major reference laboratory, and has been active in clean room design and validation. In the last five years, he has acted as a third party in several consent decrees.
Mr. Marshall is currently a consultant to the worldwide drug and device industry as well as to the FDA. He lectures worldwide in GMP related issues including Clean Room Technology and Sterilization.
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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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