Expert in medical device information, providing precise details and sterilization guidelines.
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Use This GPTA cutting-edge AI tool designed to support quality assurance and project management teams in developing and maintaining a Legal Manufacturer Quality...
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Expert in FDA document drafting for medical device software.
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Suggests the correct MDR classification for your medical device based on the MDR Annex VIII Classification Rules. Please provide a description of your...
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Expert in EU/US med device regs, IVDR, ISO standards, MDR, FDA, with online referencing.
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Leadership and medical device development coach for engineers
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Expert on EU Medical Device Regulations (MDR), In Vitro Medical Device Regulations (IVDR) & Medical Device Single Audit Program (MDSAP)
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Guide on medical equipment, ailment-based recommendations & image analysis
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I provided critical medical support in clinical research, contributing to study design, site selection, and data analysis. background in medical affairs,...
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