Process Validation for Biopharmaceuticals 2010
March 1 - 2, 2010
Carlsbad , Vereinigte Staaten
We are entering a new era of process validation due to recent changes in regulatory expectations that will have a dramatic impact on your process validation efforts. At the center of these changes is the implementation of Quality by Design (QbD) which requires a higher degree of process understanding and control.
IBC's Process & Product Validation will give you the information you need to achieve a better process understanding. Our 2010 agenda, will give you a first-hand look at how companies are going to overcome the daunting challenge of capturing and transferring all that information once the paradigm is changed to a QbD approach. Plus, extensive case studies will provide you with prospective and retrospective on the latest tools & approaches to ensure successful process and product validation.
"Great conference with many valuable topics covered"
IBC's Process & Product Validation will give you the information you need to achieve a better process understanding. Our 2010 agenda, will give you a first-hand look at how companies are going to overcome the daunting challenge of capturing and transferring all that information once the paradigm is changed to a QbD approach. Plus, extensive case studies will provide you with prospective and retrospective on the latest tools & approaches to ensure successful process and product validation.
"Great conference with many valuable topics covered"
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