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HUM-MOLGEN
-> Events
-> Courses and Workshops |
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March 11, 2014 |
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CfPA-The Center for Professional Advancement, 90 Minute Accredited Online Training
April 8, 2014 at 11:00 a.m.–12:30 p.m. (ET)
Who Should Attend
This course is designed for professionals in the life science industries especially for those working in Pharmaceutical, Medical Device and Biotech companies. It will be particularly valuable to those engaged in the following:
• Quality Assurance
• Audit
• Production
• Engineering
• Maintenance
• Architectural
• Construction Description
This course will be available On Demand: April 9, 2014
This 90-minute accredited training course will offer a basic understanding of the fundamentals of the sterile products manufacturing environment.
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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 Marshall; President, William G. Marshall and 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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