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pda第,54号报告.doc

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pda第,54号报告

pda第,54号报告 pda技术报告目录 PDA的技术报告目录 PDA——Parenteral Drug Association，注射用药物协会（/retype/zoom/e7a1cef7ba0d4a7302763a4b?pn=1x=0y=0raww=40rawh=19o=png_6_0_0_0_0_45_21_892.979_1262.879type=picaimh=19md5sum=e43571b708f597ab1c5f81ba88d1e5f6sign=6e885595dbzoom=png=0-199jpg=0-0” target=“_blank”点此查看 Technical Report No.20 - Report on Survey of Current Industry Gowning Practices Technical Report No.21 - Bioburden Recovery Validation Technical Report No.22 - Process Simulation Testing for Aseptically Filled Products Technical Report No.23 - Industry Survey on Current Sterile Filtration Practices Technical Report No.24 - Current Practices in the Validation of Aseptic Processing 1996 Technical Report No.25 - Blend Uniformity Analysis: Validation and In-Process Testing Technical Report No.26 - Sterilizing Filtration of Liquids Technical Report No.27 - Pharmaceutical Package Integrity Technical Report No.28 - Process Simulation Testing for Sterile Bulk Pharmaceutical Chemicals Technical Report No.29 - Points to consider for Cleaning Validation Technical Report No.30 - Parametric Release of Pharmaceuticals Terminally Sterilized by Moist Heat Technical Report No.31 - Validation amp; Qualification of Computerized Laboratory Data Acquisition Systems Technical Report No.32 - Auditing of Suppliers Providing Computer Products and Services for Regulated Pharmaceutical Operations Technical Report No.33 - Evaluation, Validation amp; Implementation of New Microbiological Testing Methods Technical Report No.34 - Design and Validation of Isolator Systems for the Manufacturing and Testing of Health Care Products Technical Report No.35 - A Proposed Training Model for the Microbiological Function in the Pharmaceutical Industry Technical Report No.36 - Current Practices in the Validation of Aseptic Processing - 2001 Technical Report No.39 - Cold Chain Guidance for Medicinal Products: Maintaining the Quality of Temperature-Sensitive Medicinal Products Through the Transportation Environment Technical Repor