[1] FDA. CDER Offices and Divisions [EB/OL]. 2014-05-20[2014-06-01]. http://www.fda.gov/AboutFDA/Centers Offices/OfficeofMedicalProductsandTobacco/CDER/ucm075128.htm
[2] Deborah, B.L. J. Drug Alcohol. Depen. 2009, 105S, S9-S13.
[3] FDA. Significant Dates in U.S. Food and Drug Law History [EB/OL]. 2014-03-25 [2014-04-29]. http://www.fda.gov/AboutFDA/WhatWeDo/History/Milestones/ucm128305.htm
[4] Ning, Y,Y.; Yang,Y. J. Chin. J. New Drugs. 2010, 23, 2120-2123.
[5] FDA. Adverse Event Reporting System (FAERS) (formerly AERS) [EB/OL]. 2012-09-10 [2014-04-29]. http://www.fda.gov/Drugs/GuidanceComplianceRegulatory Information/Surveillance/AdverseDrugEffects/default.htm
[6] FDA. Management the Risks from Medical Product Use—Creating a Risk Management Framework [EB/OL]. 1999-05 [2014-04-29]. http://www.fda.gov/downloads/safety/safetyofspecificproducts/ucm180520.pdf
[7] FDA. PDUFA Legislation and Background [EB/OL]. 2013-02-22 [2014-04-29]. http://www.fda.gov/ForIndustry/UserFees/PrescriptionDrugUserFee/ucm144411.htm
[8] FDA. PDUFA Legislation and Background: PDUFA II[EB/OL]. 2011-02-16 [2014-04-29]. http://www.fda.gov/ForIndustry/UserFees/PrescriptionDrugUserFee/ucm 145396.htm
[9] FDA. White Paper Prescription Drug User Fee Act (PDUFA): Adding Resources and Improving Performance in FDA Review of New Drug Applications [EB/OL]. 2010-05-03 [2014-04-29]. http://www.fda.gov/ForIndustry/UserFees/PrescriptionDrugUserFee/ucm119253.htm
[10] FDA. Guidance for Industry Premarketing Risk Assessment [EB/OL]. 2005-03 [2014-04-29]. http://www.fda.gov/downloads/drugs/guidancecomplianceregulatoryinformation/guidances/ucm072002.pdf
[11] FDA. Guidance for Industry Development and Use of Risk Minimization Action Plans [EB/OL]. 2005-03[2014-04-29]. http://www.fda.gov/downloads/drugs/guidancecomplianceregulatoryinformation/guidances/ucm071616.pdf
[12] FDA. Guidance for Industry Good Pharmacovigilance Practices and Pharmacoepidemiologic Assessment [EB/OL]. 2005-03 [2014-04-29]. http://www.fda.gov/downloads/drugs/guidancecomplianceregulatoryinformation/guidances/ucm071696.pdf
[13] FDA. GuidanceDrug Safety Information-FDA’s Communication to the Public [EB/OL]. 2007-03 [2014-04-29]. http://www.fda.gov/downloads/drugs/guidancecompliancere gulatoryinformation/guidances/ucm072281.pdf
[14] FDA. Full Text of FDAAA Law [EB/OL]. 2009-08-17[2014-04-29]. http://www.fda.gov/RegulatoryInformation/Legislation/FederalFoodDrugandCosmeticActFDCAct/SignificantAmendmentstotheFDCAct/FoodandDrug AdministrationAmendmentsActof2007/FullTextofFDAAA Law/default.htm
[15] FDA. Food and Drug Administration Amendments Act (FDAAA) of 2007 [EB/OL]. 2011-12-02 [2014-04-29]. http://www.fda.gov/RegulatoryInformation/Legislation/FederalFoodDrugandCosmeticActFDCAct/Significant AmendmentstotheFDCAct/FoodandDrugAdministration AmendmentsActof2007/default.htm
[16] FDA. PDUFA Legislation and Background: PDUFA IV[EB/OL]. 2011-09-19 [2014-04-29]. http://www.fda.gov/ ForIndustry/UserFees/PrescriptionDrugUserFee/ucm 145390.htm
[17] FDA. Prescription Drug User Fee Act (PDUFA) IV Drug Safety Five-Year Plan [EB/OL]. 2008-12 [2014-04-29]. http://www.fda.gov/downloads/ForIndustry/UserFees/PrescriptionDrugUserFee/UCM119244.pdf
[18] FDA. PDUFA V: Fiscal Years 2013 - 2017 [EB/OL]. 2013-12-26 [2014-04-29]. http://www.fda.gov/ForIndustry/UserFees/PrescriptionDrugUserFee/ucm272170.htm
[19] FDA. FDA Basics Webinar: A Brief Overview of Risk Evaluation and Mitigation Strategies (REMS) [EB/OL]. 2014-06-02 [2014-06-02]. http://www.fda.gov/AboutFDA/Transparency/Basics/ucm325201.htm
[20] FDA. FDA published Guidance Medication Guides— Distribution Requirements and Inclusion in Risk Evaluation and Mitigation Strategies (REMS) [EB/OL]. 2011-11 [2014-04-29]. http://www.fda.gov/downloads/drugs/guidancecomplianceregulatoryinformation/guidances/ucm244570.pdf2011-11
[21] FDA. Risk Communication [EB/OL]. 2012-08-03 [2014-04-29]. http://www.fda.gov/ScienceResearch/SpecialTopics/RiskCommunication/default.htm
[22] FDA. Strategic Plan for Risk Communication [EB/OL]. 2012-12-14 [2014-04-29]. http://www.fda.gov/AboutFDA/ReportsManualsForms/Reports/ucm183673.htm
[23] FDA. Communicating Risks and Benefits: An Evidence-Based User's Guide [EB/OL]. 2011-08-18 [2014-04-29]. http://www.fda.gov/AboutFDA/ReportsManualsForms/Reports/ucm268078.htm
[24] FDA. Postmarket Drug Safety Information for Patients and Providers [EB/OL]. 2012-3-08 [2014-04-29]. http://www.fda.gov/Drugs/DrugSafety/Postmarket DrugSafetyInformationforPatientsandProviders/default.htm
[25] Quan, M.; Yang, S.; Li, Y.Y.; Hou, Z.X.; Jiang, B. J. Chin. Pharm. Sci. 2013, 6, 503-507.
[26] Huang, X.W.; Lv, Y.L.; Shi, L.W.; Jiang, B. J. Chin. Pharm. Sci. 2009, 18, 278-282.
[27] National Center for ADR Monitoring [EB/OL] [2014-04-29]. http://www.cdr.gov.cn/
[28] Bi, L.Y.; Yang, Y. J. Chin. J. New Drugs. 2011, 12, 1061-1064.
[29] Hu, M.; Chen, Q.J.; Wu, P. J. Chin. Pharm. Sci. 2010, 21, 685-687. |