MARC

Tag First Indicator Second Indicator Subfields
LEADER 00000cam a2200000Ia 4500
001 in00002492447
005 20211202191529.0
006 m d f
007 cr an|||||||||
008 090504s2007 mdua ob f000 0 eng d
035 |a (OCoLC)ocn320127254 
040 |a GPO  |c GPO  |d GPO  |d MvI  |d UtOrBLW 
043 |a n-us--- 
049 |a WWW 
074 |a 0499-T-02 (online) 
086 0 |a HE 20.4802:V 83/2/DRAFT 
245 0 0 |a In vitro diagnostic (IVD) device studies, frequently asked questions. 
246 1 |i At head of title:  |a Draft guidance for industry and FDA staff 
264 1 |a Rockville, MD :  |b U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Devices and Radiological Health :  |b Center for Biologics Evaluation and Research,  |c [2007] 
300 |a 1 online resource (ii, 46 pages) :  |b digital, PDF file. 
336 |a text  |b txt  |2 rdacontent 
337 |a computer  |b c  |2 rdamedia 
338 |a online resource  |b cr  |2 rdacarrier 
500 |a Title from PDF title page (viewed on May 4, 2009). 
500 |a "Document issued on: October 25, 2007". 
504 |a Includes bibliographical references: (pages 30-32). 
500 |a Electronic resource. 
650 0 |a Toxicity testing  |x In vitro  |z United States. 
650 0 |a Medical instruments and apparatus  |z United States  |x Testing. 
710 2 |a Center for Devices and Radiological Health (U.S.) 
710 2 |a Center for Biologics Evaluation and Research (U.S.) 
856 4 0 |u https://purl.fdlp.gov/GPO/LPS112196  |t 0 
999 |a MARS 
999 f f |s 2977a81a-bb41-3091-a1ce-122a400146a5  |i 075753df-2e9b-37cc-b8fa-a83660c17df2  |t 0 
952 f f |a Texas A&M University  |b College Station  |c Electronic Resources  |d Available Online  |t 0  |e HE 20.4802:V 83  |h Superintendent of Documents classification 
998 f f |a HE 20.4802:V 83  |t 0  |l Available Online