Succeed with the Tougher U.S. FDA cGMP Compliance Audits
November 13, 2012 - Palo Alto CA US
This 90-minute webinar will evaluate the chief areas of an FDA CGMP compliance audit and help you understand the actual and anticipated changes in emphasis based on this new regulatory climate. It will prepare you and your company for tougher US FDA audits. Areas Covered in the Seminar: - The "target". - Avoid complacency from past "good" U.S. FDA/ EU ISO audits. - The desired response. - How to respond now -- where to shift focus first. - Where to direct scarce resources. - A risk-based phased approach. - Prove 'in control'. - Maintain 'the edge'. Event Details: Date: November 13, 2012 Time: 10:00 AM-11:30 AM PDT Cost: $299 per attendee per computer terminal Registration: SIgn-Up on-line now. Add to your shopping cart.