Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Sharon S. Ehrmeyer"'
Autor:
Sharon S. Ehrmeyer
Publikováno v:
Türk Biyokimya Dergisi, Vol 31, Iss 4, Pp 161-163 (2006)
In the U.S., all clinical laboratory testing is regulated by the Clinical Laboratory Improvement Amendments (CLIA). CLIA links test quality and adherence to a body of testing regulations intended to ensure accurate, reliable and timely patient test r
Externí odkaz:
https://doaj.org/article/d1e746365dcc413a9c37ee94aef83a10
Publikováno v:
The Journal of Applied Laboratory Medicine. 5:480-493
BackgroundPoint-of-care testing (POCT) continues to expand worldwide. Concerns remain about result quality despite guidelines and standards that specify testing practices. To better understand POCT testing worldwide, we polled analysts to obtain thei
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a98134afd7c7ecbaba42a8fb1459469
https://doi.org/10.1093/jalm/jfaa037
https://doi.org/10.1093/jalm/jfaa037
Publikováno v:
Clinical Biochemistry. 50:1330-1331
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::adca9663c736b29b07a7ac7e2b805273
https://doi.org/10.1016/j.clinbiochem.2017.07.019
https://doi.org/10.1016/j.clinbiochem.2017.07.019
Autor:
Sharon S. Ehrmeyer
Publikováno v:
Clinics in Laboratory Medicine. 33:27-40
The Clinical Laboratory Improvement Amendments of 1988 (CLIA) requires all US clinical laboratories that test "materials derived from the human body for the purpose of providing information for the diagnosis, prevention, or treatment of any disease..
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41f1934cfd2f1645e73d863a1af4792a
https://doi.org/10.1016/j.cll.2012.11.007
https://doi.org/10.1016/j.cll.2012.11.007
Autor:
Sharon S. Ehrmeyer
Publikováno v:
Point of Care: The Journal of Near-Patient Testing & Technology. 10:59-62
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::df06c2f96a5f974b79ac1b158ea3f5a1
https://doi.org/10.1097/poc.0b013e31821bd6af
https://doi.org/10.1097/poc.0b013e31821bd6af
Autor:
Ronald H. Laessig, Sharon S. Ehrmeyer
Publikováno v:
Clinics in Laboratory Medicine. 29:463-478
All clinical laboratory testing in the United States is regulated by the Clinical Laboratory Improvement Amendments of 1988 (CLIA'88 or CLIA) and overseen by the Centers for Medicare and Medicaid Services. CLIA profoundly changed the prevailing Unite
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4303f221271cc835076d6963489cfcd
https://doi.org/10.1016/j.cll.2009.06.012
https://doi.org/10.1016/j.cll.2009.06.012
Autor:
Sharon S. Ehrmeyer, Ronald H. Laessig
Publikováno v:
Accreditation and Quality Assurance. 13:139-144
Auditing of clinical laboratories is a recognized component of quality assurance practice. National regulatory standards, such as the U.S. Clinical Laboratory Improvement Amendments (CLIA), and international voluntary standards, such as those promulg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf7237d09473cbc181a1c86d7d6e3fcf
https://doi.org/10.1007/s00769-007-0337-7
https://doi.org/10.1007/s00769-007-0337-7
Autor:
Sharon S. Ehrmeyer, Ronald H. Laessig
Publikováno v:
Accreditation and Quality Assurance. 11:265-268
In the U.S., all clinical laboratory testing is regulated by the Clinical Laboratory Improvement Amendments (CLIA) (http://www.phppo.cdc.gov/clia/regs/toc.aspx). The CLIA link test quality and adherence to a body of testing regulations intended to en
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b78456b345a41e7ed20affd7652c004e
https://doi.org/10.1007/s00769-006-0126-8
https://doi.org/10.1007/s00769-006-0126-8
Publikováno v:
Point of Care: The Journal of Near-Patient Testing & Technology. 4:146-149
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b35f7485be631e94300cf1445926216f
https://doi.org/10.1097/01.poc.0000189932.27601.ff
https://doi.org/10.1097/01.poc.0000189932.27601.ff
Autor:
Sharon S. Ehrmeyer, Ronald H. Laessig
Publikováno v:
Clinica Chimica Acta. 346:37-43
Background: The Clinical Laboratory Improvement Amendments of 1988 (CLIA'88) mandate universal requirements for all U.S. clinical laboratory-testing sites. The intent of CLIA'88 is to ensure quality testing through a combination of minimum quality pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0fa3c0d027cd0fd932246456491c09c7
https://doi.org/10.1016/j.cccn.2003.12.033
https://doi.org/10.1016/j.cccn.2003.12.033