LEADER 01841nam 2200373Ia 450 001 9910698901103321 005 20090430151133.0 035 $a(CKB)5470000002396850 035 $a(OCoLC)319711616 035 $a(EXLCZ)995470000002396850 100 $a20090430d2008 ua 0 101 0 $aeng 135 $auran||||||||| 181 $ctxt$2rdacontent 182 $cc$2rdamedia 183 $acr$2rdacarrier 200 00$aQ4B, annex 3, evaluation and recommendation of pharmacopoeial texts for use in the ICH regions on test for particulate contamination, sub-visible particles$b[electronic resource] /$fInternational Conference on Harrmonisation of Technical Requrements for Registration of Pharmaceuticals for Human Use 210 1$a[Rockville, MD] :$c[U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Biologics Evaluation and Research],$d[2007] 215 $a7 unnumbered pages $cdigital, PDF file 300 $aTitle from PDF title page (viewed on Apr. 30, 2009). 300 $a"Draft consensus guideline". 300 $a"Current step 2 version, dated November 1, 2007". 320 $aIncludes bibliographical references: (page [4]). 517 3 $aEvaluation and recommendation of pharmacopoeial texts for use in the ICH regions on test for particulate contamination, sub-visible particles 606 $aDrugs$xMicrobiology$xTesting 615 0$aDrugs$xMicrobiology$xTesting. 712 02$aCenter for Biologics Evaluation and Research (U.S.) 712 12$aInternational Conference on Harmonisation. 801 0$bGPO 801 1$bGPO 906 $aBOOK 912 $a9910698901103321 996 $aQ4B, annex 3, evaluation and recommendation of pharmacopoeial texts for use in the ICH regions on test for particulate contamination, sub-visible particles$93191535 997 $aUNINA