LEADER 01948oam 2200433Ia 450 001 9910698737203321 005 20091223162307.0 035 $a(CKB)5470000002396485 035 $a(OCoLC)318814007 035 $a(EXLCZ)995470000002396485 100 $a20090420d2008 ua 0 101 0 $aeng 135 $auran||||||||| 181 $ctxt$2rdacontent 182 $cc$2rdamedia 183 $acr$2rdacarrier 200 00$aQ4B evaluation and recommendation of pharmacopoeial texts for use in the ICH regions$b[electronic resource] $eannex 5, disintegration test general chapter 210 1$a[Silver Spring, MD] :$c[Center for Drug Evaluation and Research] ;$a[Rockville, MD]:$c[U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Biologics Evaluation and Research],$d[2008] 215 $a5 unnumbered pages $cdigital, PDF file 300 $aTitle from PDF title page (viewed on Apr. 20, 2009). 300 $a"International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use"--p. [2]. 300 $a"Draft consensus guideline." 300 $a"Current step 2 version, dated June 5, 2008." 320 $aIncludes bibliographical references (page [4]). 517 $aQ4B evaluation and recommendation of pharmacopoeial texts for use in the ICH regions 606 $aTablets (Medicine)$xTesting 606 $aCapsules (Pharmacy)$xTesting 615 0$aTablets (Medicine)$xTesting. 615 0$aCapsules (Pharmacy)$xTesting. 712 02$aCenter for Drug Evaluation and Research (U.S.) 712 02$aCenter for Biologics Evaluation and Research (U.S.) 712 12$aInternational Conference on Harmonisation. 801 0$bGPO 801 1$bGPO 801 2$bGPO 906 $aBOOK 912 $a9910698737203321 996 $aQ4B evaluation and recommendation of pharmacopoeial texts for use in the ICH regions$93471792 997 $aUNINA