In our latest panel discussion, Standardizing stool sampling: Value of FDA authorization, we disseminate the device’s journey in receiving FDA authorization and why this designation is important for diagnostic and therapeutic assay developers.
Hear from our team of experts from Regulatory Affairs, Product Management and Research & Development on:
Collect superior samples for your microbiome analysis, increase donor compliance and improve efficiency through reduced validation time and proven reproducibility with the OMNIgene• GUT Dx device.