LEADER 01747cam  2200409Ia 4500001    ocn489146378
003    OCoLC
005    20091215164304.0
006    m        d f      
007    cr a||||||||||
008    091215s1999    mdu     o    f000 0 eng d
040    GPO |cGPO |dMvI
043    n-us---
049    ERE#
074    0499-T (online)
086 0  HE 20.4702:T 28
245 00 Guidance for industry : |bQ6B specifications : test procedures and acceptance criteria for biotechnological /biological products.
246 30 Q6B specifications
246 30 Test procedures and acceptance criteria for biotechnological /biological products
260    Rockville, MD : |bU.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research : |bCenter for Biologics Evaluation and Research, |c[1999]
300    1 online version (21 p.)
336    text |btxt |2rdacontent
337    computer |bc |2rdamedia
338    online resource |bcr |2rdacarrier
500    "ICH."
500    "August 1999."
500    GPO Cataloging Record Distribution Program (CRDP).
650  0 Biotechnology |xResearch |xStandards |xInternational cooperation. |=^A225126
650  0 Biological products |xTesting. |=^A132664
710 2  Center for Drug Evaluation and Research (U.S.) |=^A431016
710 2  Center for Biologics Evaluation and Research (U.S.) |=^A368272
711 2  International Conference on Harmonisation. |=^A998855
856 40  |uhttps://purl.fdlp.gov/GPO/LPS117741
949    Click on web address |wasis |hjoyner94
596    1
998    2189685