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狼行拂晓
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美国GDUFA中立卷审查(GDUFA INITIAL COMPLETENESS ASSESSMENT CHECKLIST FOR TYPE II API DMFs)的评审建议,同时要结合不接受标准ANDA Submissions –Refuse-to-Receive Standards Guidance for Industry: 3.2.S.2.1 Contains complete Manufacturer Information on the following for each site: Note: If a late stage intermediate has been outsourced, detailed information regarding the source for each supplier needs to be provided in section 2.3. Separate facilities used for release testing of the API and for additional processing (e.g. micronization) should also be listed. Central File Number or Facility Establishment Identifier numbers should be provided if available. 3.2.S.2.2 Contains Description of Manufacturing Process and Process Controls addressing the following: Note: DMF will not be considered complete for review requirements if the complete process is not included in the DMF or by appropriate reference to another DMF. If the firm chooses intermediates as “starting materials” a determination should be made if information is provided in the DMF to adequately evaluate their controls and effect on the drug substance quality and purity. 3.2.S.2.3 Contains information on the Control of Materials, as follows: Note: Specification, analytical protocol and representative CoA of each reagent/solvent should be provided. 3.2.S.2.4 Contains information for Controls of Critical Steps and Intermediates as follows: For sterile APIs. 3.2.S.4 Information is provided to support the Control of the Drug Substance as follows: Method validation reports may be included in section 3.2.R.3.S. |

10楼2015-10-12 22:49:57
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2楼2015-10-09 22:23:35
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3楼2015-10-11 09:07:20
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5楼2015-10-11 12:45:41












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