Terms and Conditions
  1. Physician has read and understands the PDGFRB Product Datasheet.
  2. Physician agrees to comply with FDA-approved device labeling.
  3. Physician agrees to comply with pertinent state and federal regulations.
  4. Physician agrees to comply with national IRB requirements.
  5. Physician acknowledges that the PDGFRB Humanitarian Use Device is subject to 21 CFR Part 803 Medical Device Reporting (MDR) and will notify ARUP Laboratories of any adverse device effects.
  6. Physician, to the best of their ability, will protect the rights, safety and welfare of the patient for whom the PDGFRB assay is ordered.