Medical Device Regulations Software In USA
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by Centaur Labsbased in USA
90% of all healthcare data is medical images. Whether generated by smartphones or regulated medical imaging devices, this imaging data represents a significant opportunity for AI development. Our annotation platform enables clients to structure medical images by both classifying images and segmenting regions of ...
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based in USA
We are a regulated Software as a Medical Device (SaMD)-focused biotechnology company that develops our applications as medical treatments in accordance with all relevant FDA, ISO and IEC ...
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Manufactured by BioT Medicalbased in ISRAEL
Transform your medical devices into connected care solutions in a single day with our regulated cloud ...
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based in USA
OOS Software to Automate Out of Specification (OOS) Processes to Comply with FDA CGMPs and 21 CFR Part 211 and Part 820 Regulations. In the FDA environment, specifications are essential in maintaining quality. CGMP regulations for finished pharmaceuticals (21 CFR Parts 210-211) and medical devices (21 CFR Part 820) require strict ...
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