This change control webinar will discuss the change control activities and documentation required to meet GMP requirements
Areas Covered in the Seminar:

• Defining a "change" and "change control".
• Tougher FDA Expectations / Requirements.
• Areas impacted.
• FDA "Hot Buttons".
• Design Control.
• Document Control; Archiving.
• Identifying "changes".
• Preventing negative changes and entropy.
• Maintain a ‘state of control'.

Who Will Benefit:
This information applies to personnel / companies in the Pharmaceutical, Medical Device, Diagnostic, Neutraceutical and Biologics fields. The employees who will benefit include:

• Senior management
• Regulatory affairs
• Quality Assurance / QAE
• Production
• Engineering, R&D, and software development and testing teams

For More Information:
http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=701741?channel=biofind