| Record ID | marc_nuls/NULS_PHC_180925.mrc:319174430:1808 |
| Source | marc_nuls |
| Download Link | /show-records/marc_nuls/NULS_PHC_180925.mrc:319174430:1808?format=raw |
LEADER: 01808cam 22003614a 4500
001 9919528430001661
005 20150423121105.0
008 030910s2004 njua f 000 0 eng
010 $a 2003020146
016 7 $a101190637$2DNLM
020 $a0937548545 (pbk.)
029 1 $aNLM$b101190637
035 $a(CSdNU)u265203-01national_inst
035 $a(OCoLC)53038749
040 $aDNLM/DLC$cDLC$dNLM$dOCLCQ$dBAKER
042 $apcc
043 $an-us---
049 $aCNUM
050 00 $aR853.C55$bN67 2004
060 00 $a2005 A-549
060 10 $aQV 39$bN854c 2004
082 00 $a610/.7/2$222
100 1 $aNorris, Deborrah.
245 10 $aClinical research coordinator handbook /$cDeborrah Norris.
250 $a3rd ed.
260 $aMedford, N.J. :$bPlexus Pub.,$cc2004.
300 $ax, 144 p. :$bill. ;$c28 cm.
505 0 $aFederal regulations governing the obligations of clinical investigators of regulated articles -- The clinical research organization -- Investigator responsibilities -- Duties of the clinical research coordinator -- The creation of study source documents -- Obtaining consents, approvals, and signatures -- Pertinent forms and study records -- The prestudy site visit -- Recruiting and enrolling subjects -- Conducting the study and keeping records -- Preparing for an fda audit -- Clinical research: potential liability -- Writing the study summary -- Achieving credibility and recognition as a clinical research coordinator.
650 0 $aClinical trials$zUnited States$vHandbooks, manuals, etc.
938 $aBaker & Taylor$bBKTY$c39.95$d44.90$i0937548545$n0004315458$sactive
949 $aR 853.C55 N67 2004$i31786102053466
994 $a92$bCNU
999 $aR 853 .C55 N67 2004$wLC$c1$i31786102053466$d9/6/2013$e8/5/2013 $lCIRCSTACKS$mNULS$n1$rY$sY$tBOOK$u2/9/2006