A week after an international group of journalists published a package of stories slamming the medical device industry, the FDA has issued its own report highlighting its accomplishments dating back to 2007.
The Medical Device Enforcement and Quality Report touts:
- Increased medtech manufacturer inspections and voluntary reporting of violative devices and adverse events;
- Targeted enforcement of regulations regarding particular devices;
- Firms’ corrective actions following inspections; and
- The use of regulations to promote device quality, not just compliance, through its Case for Quality pilot program launched this year.
Get the full story on our sister site, Medical Design & Outsourcing.
The post FDA tells its side of regulatory, quality story appeared first on MassDevice.
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