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Date: 2nd July, 2009

Location: On-Line, USA

Summary:
Pharmaceutical - Training

Click here to Register for this Seminar

It is the goal of every manufacturing firm to maximize profit. This is often accomplished by process automation. Domestic and international regulations contain the requirements to verify that the process yields output that is both safe and effective, and meets all requirements. These requirements are also applicable to manual, "un-automated" processes. This webinar will set forth the regulatory requirements for process validation, and will also include definitions and application of applicable terminology, and hints and recommendations for the more common types of process validation. These recommendations will address the challenges most commonly experienced during validation. Also covered will be the validation technique used for processes that are already in place.

Areas Covered in the seminar:

• What is Validation?
  
• When should it be used?
  
• Validation vs. Verification: Which One?
  
• Different types of validation: Advance, retrospective, and concurrent
  
• Protocol preparation.
  
• Different types of validation.
  
• IQ, OQ, and PQ.
  
• Case studies and examples.
  

Process Validation Principles and Protocols