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Cleanroom Qualification Protocol

 
  October 26, 2017  
     
 
CfPA-The Center for Professional Advancement, Online Live
December 7, 2017 at 11:00 a.m.–12:00 p.m. (ET)


Who Should Attend?
This online training has been developed for Personnel that work in, develop procedures for, monitor, provide technical support for, and design cleanrooms. Professionals who will benefit greatly from this training include personnel in:

  • QA, QC
  • Production
  • Engineering 
  • Maintenance
  • Architects
  • Development 

In addition, Cleanroom Contractors and Engineers involved in designing and constructing cleanrooms will find the course extremely worthwhile. 

Course Description
This 60-minute online training course will outline the necessary steps needed to qualify a cleanroom. It will provide a format for writing the Qualification Protocol. The training will address the execution of the protocol and highlight mitigation of common problems.

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: December 8, 2017
 
 
Organized by: CfPA-The Center for Professional Advancement
Invited Speakers:

   William Marshall, President, William G. Marshall and Associates

William G. Marshall is President of William G. Marshall and Associates. He has over forty years of 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. In the past 18 months, he has been involved in 10 Pre- Approval Inspections that include the first aseptic processed injectables from India, the first ever drugs from Turkey, and APIs from China, that were all approved for introduction to the US market. He has a Master’s Degree in Biology from Georgetown University, Washington, DC.

Mr. Marshall’s training continues to receive CfPA’s most highly rated reviews. He liberally uses Case Studies from Warning Letters and Consent Decrees and his 40 plus years working in manufacturing and consulting in over 25 countries. Attendees are encouraged to question , debate , and share their own problems and successes. Mr. Marshall’s style of training is to keep the course very interactive. Attendees find his enthusiasm, knowledge, and experience, wrapped in a sense of humor, stimulating as well as informative. 

 


 
Deadline for Abstracts: n/a
 
Registration: Please click here for registration information.
E-mail: jmorbit@cfpa.com
 
   
 
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