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TEDMED Engineering and Projects.


FDA MEDICAL DEVICE CLASSIFICATION
The Food and Drug Administration also known as (FDA), created about 1700 classification for different types of generic devices. They also...
bbonsu549
Nov 12, 20232 min read
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FDA Guidelines AND ICH GCP Standards
Companies cannot market new drugs, medical devices, or biological products, without providing to the U.S. Food and Drug Administration...
bbonsu549
Nov 12, 20232 min read
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