These resource pages are intended to explain some terms and concepts important for the evaluation of biocompatibility of medical devices| U.S. Food and Drug Administration
The International Organization for Standardization released ISO 10993-17. This document specifies the toxicological risk evaluation process of medical devices.| Vantage Medtech
With a scarcity of organ donors all over the world, and their ability to expedite the recovery process, the demand for implantable medical devices is increasing rapidly.| Vantage Medtech
Before you hire a medical device outsourcing company, do your due diligence, ask the right questions, and learn as much as you can about them to ensure they are the right fit.| Vantage Medtech
Our clients know they want to produce a high-quality device but are unaware of an element essential to good manufacturing practices for medical devices – risk management.| Vantage Medtech