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 |
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Pages (from-to) | 332-333 |
Number of pages | 2 |
Journal | Nature Reviews Urology |
Volume | 16 |
Issue number | 6 |
DOIs |
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State | Published - 1 Jun 2019 |
Externally published | Yes |