01872nam 2200421Ia 450 991069890510332120090727154356.0(CKB)5470000002398829(OCoLC)427904766(EXLCZ)99547000000239882920090727d2001 ua 0enguran|||||||||txtrdacontentcrdamediacrrdacarrierGuidance for industry[electronic resource] 21 CFR part 11, electronic records, electronic signatures, validationRockville, MD :U.S. Dept. of Health and Human Services, Food and Drug Administration, Office of Regulatory Affairs :Center for Biologics Evaluation and Research :Center for Drug Evaluation and Research :Center for Devices and Radiological Health :Center for Food Safety and Applied Nutrition :Center for Veterinary Medicine,[2001]iii, 21 pages digital, PDF fileTitle from PDF title page (viewed on July 27, 2009)."Draft guidance"."August 2001".Includes bibliographical references (pages 15-21).Guidance for industry Electronic recordsGovernment policyUnited StatesElectronic recordsGovernment policyUnited States.Food and Drug Administration.Office of Regulatory Affairs.Center for Biologics Evaluation and Research (U.S.)Center for Drug Evaluation and Research (U.S.)Center for Devices and Radiological Health (U.S.)Center for Food Safety and Applied Nutrition (U.S.)Center for Veterinary Medicine (U.S.)GPOGPOBOOK9910698905103321Guidance for industry3434577UNINA