01556nam 2200421Ia 450 991069897970332120090617145026.0(CKB)5470000002398076(OCoLC)401784386(EXLCZ)99547000000239807620090617d2001 ua 0enguran|||||||||txtrdacontentcrdamediacrrdacarrierGuidance for industry[electronic resource] Q7A good manufacturing practice guidance for active pharmaceutical ingredientsRockville, MD :U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research :Center for Biologics Evaluation and Research,[2001]iv, 52 pages digital, PDF fileTitle from PDF title page (viewed on June 17, 2009)."ICH"."August 2001".Guidance for industry Drug factoriesQuality controlPharmaceutical chemistryDrugsQuality controlDrug factoriesQuality control.Pharmaceutical chemistry.DrugsQuality control.Center for Drug Evaluation and Research (U.S.)Center for Biologics Evaluation and Research (U.S.)International Conference on Harmonisation.GPOGPOBOOK9910698979703321Guidance for industry3434577UNINA