White Paper: Labeling In Vitro Diagnostic Products - 5 Best Practices to Ensure Compliance with FDA Regulations

• By: ComplianceOnline
• Date: July 07, 2014

The FDA has been cracking down on non-compliance in vitro diagnostic products or IVDs recently. Manufacturers have not been adhering to the strict regulations governing the use of these products, and have been falling short when it comes to the compliant labeling of these devices. This White Paper puts together five best practices that can help IVD manufacturers improve their compliance with labeling and avoid FDA citations, Warning Letters, product recalls and worse.

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