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Process Validation for Drugs and Biologics

  December 19, 2013  
Center for Professional Innovation & Education, Inc., Malvern, PA
Feb. 10 & 11, 2014

The application of Process Validation is becoming an increasingly important activity for pharmaceutical and biotech organizations given the critical role validated processes have in ensuring product conformance.   To assist industry, several guidances have been developed by regulatory agencies in the last few years that define the requirements and best practices for the effective implementation of Process Validation. 

Organizations that fail to develop an effective process validation system will face significant regulatory consequences including For Cause audits by regulators, recalls or plant closure.  However, the application of process validation is not limited to the manufacturer; it also extends to include suppliers.  Regulations have been established which direct organizations to assess the adequacy of process validation activities at their suppliers.  For example, regulators expect organizations to begin process validation activities before new equipment is installed.

This course, entirely updated to reflect the current requirements and guidances published by the Pharmaceutical Inspection Convention and Pharmaceutical Inspection Co-operation Scheme, the European Medicines Agency , FDA and International Conference on Harmonization, will provide participants with a thorough understanding of the requirements of process validation.  They will learn how to establish an effective process validation system and integrate it with other systems such as Risk Management, Corrective and Preventive Action and Supplier Management. 

Participants will learn how to develop rigorous protocols and reports, as well as create monitoring programs to ensure that defined critical parameters remain in control.  The course will also review validation requirements for systems that generate electronic signatures and records as most new processes have this capability.  

Attendees are encouraged to bring examples of Process Validation issues/concerns that they would like to reviewed and discussed during the course.

This course has been pre-approved by the Regulatory Affairs Professionals Society (RAPS) as eligible for 12 credits towards a participant's RAC recertification upon full completion. 

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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