New White Paper: The Future of Change and Configuration Management in the Med-Tech Industry
Can you distribute poor quality products while complying with all applicable regulatory requirements? Sure! After all, you can conduct a recall of poor quality products in compliance with all applicable regulations. FDA’s Top Medical Device official agrees.
Jeff Shuren, M.D., J.D., Director of FDA’s Center for Devices and Radiological Health (CDRH), put it this way: “…one device manufacturer can meet FDA requirements and still make a poor quality device; whereas, a second manufacturer may not comply with all FDA requirements and yet make a high-quality device.”
Is your organization focused on Solving Quality Problems or Avoiding Them? Download the white paper to find out how Med-Tech Innovators have been able to shift their focus on improving market presence, manufacturing processes and product quality.
Contact: email@example.com to see if you qualify for a complimentary access code and save $499.