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001 on1161990836
003 OCoLC
005 20200902124527.0
006 m o d f
007 cr mn|||||||||
008 200701c20209999dcu x w o f0 2eng c
010 _a2020231553
040 _aGPO
_beng
_erda
_epn
_cGPO
_dMvI
042 _apcc
043 _an-us---
074 _a0807-A-09 (online)
086 0 _aLC 14.24:IF 11389/
099 _aLC 14.24:IF 11389/
100 1 _aSarata, Amanda K.,
_eauthor.
245 1 0 _aFDA regulation of laboratory-developed tests (LDTs) /
_cAmanda K. Sarata.
246 3 _aFood and Drug Administration regulation of laboratory-developed tests (LDTs)
250 _a[Library of Congress public edition].
264 1 _a[Washington, D.C.] :
_bCongressional Research Service,
_c2020-
300 _a1 online resource.
310 _aUpdated irregularly
336 _btxt
337 _bc
_2rdamedia
338 _bcr
_2rdacarrier
490 1 _aIF ;
_v11389
500 _aThe CRS report home page provides access to all versions published since 2018 in accordance with P.L. 115-141.
500 _aGPO Cataloging Record Distribution Program (CRDP).
588 _aDescription based on contents viewed on June 23, 2020; title from CRS report home page.
650 0 _aDiagnostic services
_zUnited States.
610 1 0 _aUnited States.
_bFood and Drug Administration.
710 2 _aLibrary of Congress.
_bCongressional Research Service,
_eissuing body.
773 0 8 _iContained in (work):
_tCRS reports (Library of Congress. Congressional Research Service)
_w(DLC) 2018231131
_w(OCoLC)1052784408
830 0 _aIn focus (Library of Congress. Congressional Research Service) ;
_vIF11389.
856 4 0 _uhttps://purl.fdlp.gov/GPO/gpo140660
922 _aCRSREP
922 _aCONSERNEW
_b20200701
999 _c294658
_d294658