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Brazil is rapidly establishing itself as a powerhouse in medical device innovation. This article shares market opportunities, ...

USP 382 introduces system-level, function-specific testing for elastomeric components in parenteral packaging, improving ...

Sterilization validation ensures medical device safety by confirming sterility through rigorous testing, method selection, ...

Biocompatibility assessment per ISO 10993 ensures medical device safety by evaluating materials, risks, and biological ...

The FDA has issued its much-anticipated final guidance on cybersecurity risk management in medical devices, effective June 2025.

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Recent advances in AI, including machine learning, natural language processing, and deep learning models, are transforming rare disease diagnosis.