Abstract
The FDA’s approval of the first point-of-care total PSA test for prostate cancer has the potential to improve patient care by streamlining PSA testing. However, a Clinical Laboratory Improvement Amendments waiver is needed before this test can be fully integrated into clinical care.
| Original language | English |
|---|---|
| Pages (from-to) | 332-333 |
| Number of pages | 2 |
| Journal | Nature Reviews Urology |
| Volume | 16 |
| Issue number | 6 |
| DOIs |
|
| State | Published - 1 Jun 2019 |
| Externally published | Yes |
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