The Product Recalls Forum 2018 is dedicated to Regulatory Requirements and Expectations to Minimiza the Number and Cost of Product Recalls.
The Product Recalls Forum 2018 covers topics such as:
- 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
The Product Recalls Forum 2018 brings together 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
