Product Recalls Forum 2018

The Product Recalls Forum 2018 is dedicated to Regulatory Requirements and Expectations to Minimiza the Number and Cost of Product Recalls.

Topics

• Adapting to the new medical device regulations
• How to reduce recalls in your organization
• Medical device and drug recalls and the tools to assist you in understanding the recall process
• Recent findings and the most common causes of recalls
• The fundamentals on how to effectively manage a recall in all stages from beginning to end

Who should Attend

Attendees with responsibilities in:

• Patient Safety
• Product Recalls
• Product Quality
• Product Safety
• Postmarketing Surveillance
• QA/QC
• Quality Compliance and Audits
• Quality Systems and Engineering
• Medical/Consumer/Regulatory/Clinical Affairs
• Complaint Handling
• Compliance
• Product Complaints
• Business Support Coordination
• CMO Management
• Clinical Operations
• Product Surveillance
• QA and Supply Integration
• Quality Compliance
• Drug Safety and Complaint Software Companies
• Global Device Coordination
• Law Firms
• Consulting Firms
• Inbound Call Centers