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  HUM-MOLGEN -> Events -> Courses and Workshops  

Process Validation for Drugs and Biologics

  November 28, 2011  
Center for Professional Innovation & Education (CfPIE), Dublin, Ireland
March 26 & 27 , 2012

 Participation will be beneficial to personnel directly involved in process/product development, manufacturing, quality control/assurance and process validation.  By the end of this course, attendees will be able to understand the new FDA perspective of a “Process Validation Life-Cycle” that starts at the Process Design phase (Process/Product Development) and continues through Process Qualification (Confirmation) and Continued Process Verification (Monitoring and Assessment of the process effectiveness). Additionally, participants will be able to set up effective process validation programs that meet current FDA, WHO, PIC/S and EU regulations.
Organized by: Center for Professional Innovation & Education
Invited Speakers: Contact info@cfpie.com for a list of course instructors
Deadline for Abstracts: n/a
Registration: http://www.cfpie.com/showitem.aspx?productid=049&source=hummolgen
E-mail: info@cfpie.com
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