The Quality Oversight for Medical Device Manufacturing Summit is the foremost event that brings together senior level quality executives to discuss how to ensure quality and compliance in medical device manufacturing, and offers attendees an unrivaled opportunity for learning and networking.
For any company, reviewing and understanding inspection requirements & manufacturing controls is a primary challenge. In addition, sustaining QA throughout the manufacturing processes & throughout a lifecycle of a product is critical. Through a top-down approach that integrates QA throughout an organization, companies will find fewer compliance infractions.
This event provides attendees with best practices to improve your CAPA systems, complaint & medical device reporting, and documentation processes to prevent regulatory issues. Your company will stay ahead of the curve by ensuring the quality of suppliers and understand the changing trends of the FDA and other regulatory agencies in enforcing quality oversight. This event gives you the tools to create quality products and bring them to market as quickly as possible while remaining compliant.
Top Reasons To Attend
Testimonials From Past ExL Medical Device Conferences:
“Good mix of examples, lessons learned, and discussions on challenges we are still facing.”
- Manager, Boston Scientific
“Totally relevant – very helpful examples of end results, how achieved, and learnings…”
- VP Sales, Quality Health
“Great real world examples of solutions for the sales force – with real results.”
- Manager, Medtronic
“Real examples, down to earth, and practical…”
- Global IT, Teleflex
“This is what I came here for – it was more strategy and very helpful. Thank you!”
- Business Director, Tactile Systems
This Summit is specifically designed for Medical Device professionals with responsibilities in the following areas:
This conference is also of interest to: