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GK Medtech
ygao42
Nov 63 min read
Understanding the Differences in Processing Aids and Additives for Medical Devices
When preparing regulatory documentation, distinguishing between processing aids and additives can indeed be challenging. According to...
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ygao42
Oct 101 min read
FDA draft the new guidance document "Chemical Analysis for Biocompatibility Assessment of Medical Devices Draft Guidance for Industry and Food and Drug Administration Staff"
The FDA released a draft guidance document titled "Chemical Analysis for Biocompatibility Assessment of Medical Devices Draft Guidance...
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ygao42
Sep 272 min read
Maximizing Medical Device Development Success with Comprehensive Services
In the world of medical device development, success is often synonymous with having access to comprehensive services that cover every...
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ygao42
Sep 272 min read
Accelerating Medical Device Innovation with Scientific Expertise
In the ever-evolving landscape of medical device innovation, having access to comprehensive scientific expertise can be the key to...
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ygao42
Sep 272 min read
Empowering Medical Device R&D with Regulatory and Scientific Support
In the ever-evolving landscape of medical device development, the need for robust scientific support and comprehensive regulatory...
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