Medical Device Registration & Listing, and Inspection Follow-up Activities 2015

Key Topics

• CAPAs and complaints are key focus areas during Good Manufacturing Practice (GMP) inspections and this webinar will review the ins and outs of how to manage these systems and effectively address questions FDA will likely raise
• Registration and Listing regulatory requirements, process, and how FDA uses this data will be discussed
• FDA strategic direction and how decisions are reached in developing inspection and compliance plans and how compliance actions are developed in response to violations encountered in inspections will be discussed

Who should Attend

• Regulatory Affairs managers and professionals
• VPs and Directors in Regulatory Affairs and Quality Assurance departments
• Small business owners
• Quality Managers and professionals