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A Survey of Microbiology for the Pharmaceutical, Biotechnology, and Medical Device Industries

 
  May 07, 2009  
     
 
The Center for Professional Advancement, 90 Minute Accredited Online Training
June 16, 2009 at 11:00 a.m. - 12:30 p.m. (EST)


A Survey of Microbiology for the Pharmaceutical, Biotechnology, and Medical Device Industries 
June 16, 2009 at 11:00 a.m. - 12:30 p.m. (EST) 
90 Minute Accredited Online Training

Who Should Attend
This course is intended for anyone in the medical manufacturing environment where product sterility or control of microbial contamination is essential. This includes Pharmaceutical, Biotech and Medical Device personnel in areas such as:

  • Quality Assurance
  • Maintenance
  • Production
  • Training
  • Validation
  • Purchasing
  • Technical Support

Description
This 90-minute accredited online training will address the fundamental microbiological concepts that need to be understood by staff associated with the medical products manufacturing field. The concepts will be presented in terms that will be understood by non-microbiologists. Discussions will include: personnel behavior practices, cleaning, sanitization, disinfection, and sterilization methods. In addition, the impact of raw materials (such as ingredients and packaging materials), equipment design, environment, manufacturing time frames, compressed gasses and water will be addressed. 

Module 1: What is aseptic fill, and where are aseptic fill practices required? Microbiology Basics such as:
  • Growth requirements
  • Sources of contamination
  • Disinfection
  • Sterilization

Module 2: Environmental controls:
  • Personnel issues
  • Production procedures
  • Room layout in aseptic fill operations

Module 3: Monitoring of:
  • Materials
  • People
  • Areas
  • Equipment
  • Production processes during aseptic fill
Validation
Publications
Resources

Question and Answer Session

 
 
Organized by: The Center for Professional Advancement
Invited Speakers: William Marshall; President, William G. Marshall and Associates

William G. Marshall has over twenty years experience in the Pharmaceutical and Medical Device Manufacturing Environment. Mr. Marshall has held Director level and Chief Operating Officer positions with large multinational 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.
 
Deadline for Abstracts: N/A
 
Registration: Please click here for registration information.
E-mail: salbers@cfpa.com
 
   
 
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