Pursuance of FDA draft guidance on analytical method validation for Drugs and Biologics 2014

Topics

• Acronyms
• Old and new guideline differences
• Life cycle approaches of method development
• Scope and contents of the guidance
• Validations as per new FDA guidelines

Who should Attend

• Quality assurance personnel
• Directors, Managers, Supervisors and scientists working in pharmaceuticals and food analytical laboratories
• Manufacturing plants scheduled for inspections or audits by their customers or regulatory agencies
• Laboratories scheduled for FDA approvals