[1] Sherman, R.E.; Li, J.; Shapley, S. N. Engl. J. Med. 2013, 369, 1877–1880.
[2] FDA. Review Designation Policy: Priority (P) and Standard (S) [EB/OL]. 2015-12-30. https://www.fda.gov/downloads/AboutFDA/CentersOffices/OfficeofMedicalProductsandTobacco/CDER/ManualofPoliciesProcedures/UCM082000.pdf
[3] FDA. Guidance for Industry: Expedited Programs for Serious Conditions Drugs and Biologics [EB/OL]. 2015-12-30. http://www.fda.gov/downloads/drugs/guidancecompliance-regulatoryinformation/guidances/ucm358301.Pdf
[4] FDA. Fast Track Drug Development Programs-Designation, Development, and Application Review [EB/OL]. 2015-12-30. http://www.fda.gov/BiologicsBloodVaccines/Guidance ComplianceRegulatoryInformation/ProceduresSOPPs/ucm073515.htm
[5] FDA. Investigator-Initiated Investigational New Drug (IND) Applications [EB/OL]. 2015-12-30. http://www.fda.gov/Drugs/DevelopmentApprovalProcess.htm
[6] National Food and Drug Administration Drug Special Approval Procedures (Bureau Decree No. 21) [EB/OL]. 2005-11-18. http://www.cfda.gov.cn/WS01/CL0053/24520.html
[7] Special approval of new drug registration regulations [EB/OL]. 2009-01-07. http://www.sda.gov.cn/WS01/CL0058/35157.html
[8] Definition of special approval procedures for biological products [EB/OL]. 2013-03-11. http://www.cde.org.cn/news.do?method=largeInfo&id=312958
[9] List of special approval items [EB/OL]. [2017-06-05]. http://www.cde.org.cn/news.do?method=changePage& pageName=service&frameStr=14
[10] Drugs@FDA: FDA Approved Drug Products [EB/OL]. [2017-06-05]. https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=BasicSearch.process
[11] Chen, X.Y. 2 Speed up the approval of cases of anti-tumor drugs [R]. 2017 DIA meeting, Beijing.
[12] International multicenter drug clinical trial guidelines (Trial) [EB/OL]. 2015-01-30. http://www.cde.org.cn/zdyz.do?method=largePage&id=238
[13] Center For Drug Evaluation And Research [EB/OL]. 2017-06-05. https://www.accessdata.fda.gov/drugsatfda_ docs/nda/2015/208065Orig1s000SumR.pdf
[14] Notice of the Opinions of the State Administration of Food and Drug Administration on Adjusting the Decision on the Relevant Matters Concerning the Registration of Imported Drugs (Draft for Soliciting Opinions) [EB/OL]. 2017-03-17. http://www.sfda.gov.cn/WS01/CL0778/170840.html |