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> FDA Guidance LinksMock FDA PAI AuditsFDA Guidance DocumentsImporting Directions:-Food-Drug Products-Medical DevicesContact The FDAFDA Forms - DownloadsFDA Meetings - UpcomingFDA HandbooksDrug/Device MedWatchCBER (Biologics)CDER (Drugs)Regulatory Affairs ORACDRH Medical DeviceCDRH Device AdviceHealth ProfessionalsFood - Nutrition IndustryCosmetic Industry> Condition StatesAcneADD and ADHDAIDS/HIVAllergiesAlzheimer'sArthritisAsthmaAutismBack PainBirth ControlCancer - BreastCancer - ProstateCholesterolCommon Cold | FluCrohn's & ColitisDental HealthDiabetesDiet & NutritionEar DisordersEpilepsyErectile DysfunctionGlaucomaHair LossHeadache | MigraineHeartburnHeart AttacksHepatitisHemorrhoidsKidneyLyme DiseaseMen's HealthMRSAMultiple SclerosisOsteoporosisParkinson'sSARSSIDSSkin CareSleep DisordersSmokingSnoringStress | DepressionStrokeVitaminsWeight ControlThe Weekly FDA Rule Change Newletter - Enter Email here:Our Best Sellers:21 CFR 210/211 - Drug GMPs - Complete Drug Product Regulations21 CFR 820 - Quality System Regulations - Medical Device21 CFR 112 Produce for Human Consumption21 CFR 11, 210/211, 820, ICH Q7 - cGMP Master Handbook21 CFR 11, 50, 54, 56, 807, 812, 814, 820, 510K & PMA - Medical Device Combination21 CFR 11, 50, 54, 56, 312, 314, ICH E2A, E6(R2) - Good Clinical Practice HandbookGMP International Master Reference Guide - Master cGMPs21 CFR Part 117 - Food GMPsGMP Medical Device Master Reference Guidefor assisstance with handbooks please contact John Cuspilich, Sr. Editor, at jcuspilich@fda.com. Other Best Sellers:21 CFR 3 - Combination Product Handbook - Definition, FAQ's & GMPs21 CFR 3, 4, 11, 210/211, 820, ICH Q7 - Combination Product Master21 CFR 4 - cGMP for Combination Products21 CFR 11 - Electronic Records with Scope & Application21 CFR 11 - Electronic Records with Scope & Application and Part 11 Checklist21 CFR 11 - Electronic Records with Scope & Application and Preambles21 CFR 11 - with Scope & Appl. & Computerized Systems used in Clinical Investigations21 CFR 11, 101, 110, 117, 120, 123 - GMPs for Fish Industry with Food Labeling21 CFR 11, 110, 111 and 117 - Food and Supplement GMPs21 CFR 11, 110, 117, 120 - Food GMPs21 CFR 11, 110, 117, 120, 123 - GMPs for Fish Industry21 CFR 11, 111 - Electronic Records with Dietary Supplement GMPs21 CFR 11, 203, 205 - PDMA with Electronic Records21 CFR 11, 210/211 - Electronic Records with Drug GMPs21 CFR 11, 210/211 - Electronic Records with Drug GMPs-ENGLISH/SPANISH21 CFR 11, 210/211 - Electronic Records with Drug GMPs-SPANISH21 CFR 11, 210/211 with Keyword Index21 CFR 11, 210/211, 606, 820 - Electronic Records with Drug, Blood and Device QSR21 CFR 11, 210/211, 700/701 - Cosmetic with "Is It Soap or a Drug"21 CFR 11, 210/211, 820 - Electronic Records with Drug and Device GMPs21 CFR 11, 210/211, 820 - Electronic Records with Drug and Device GMPs -ENGLISH/SPANISH21 CFR 11, 210/211, 820 - Electronic Records with Drug and Device
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