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    PDA TR 62Technical Report No. 62 (TR 62) Recommended Practices for Manual Aseptic ProcessesReport / Survey by Parenteral Drug Association, 06/01/2013

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    PDA TR 54-2Technical Report No. 54-2 (TR 54-2) Implementation of Quality Risk Management for Pharmaceutical and Biotechnology Manufacturing Operation: Annex 1: Case Study Examples for Quality Risk Management in Packaging and LabelingReport / Survey by Parenteral Drug Association, 06/01/2013

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    PDA TR 61Technical Report No. 61 (TR 61) Steam In PlaceReport / Survey by Parenteral Drug Association, 03/01/2013

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    PDA TR 60Technical Report No. 60 (TR 60) Process Validation: A Lifecycle ApproachReport / Survey by Parenteral Drug Association, 02/01/2013

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    PDA TR 29Technical Report 29, Revised 2012 (TR 29) Points to Consider for Cleaning ValidationReport / Survey by Parenteral Drug Association, 12/01/2012

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    PDA TR 3Technical Report No. 3, Revised 2013 (TR 3) Validation of Dry Heat Processes Used for Depyrogenation and SterilizationReport / Survey by Parenteral Drug Association, 07/01/2013

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    PDA TR 43 Technical Report No. 43, Revised 2013 (TR 43) Identification and Classification of Nonconformities in Molded and Tubular Glass Containers for Pharmaceutical Manufacturing:Covering Ampules, Bottles, Cartridges, Syringes & Vials Report / Survey by Parenteral Drug Association, 09/01/2013

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    PDA TR 54-3Technical Report No. 54-3 (TR 54-3) Implementation of Quality Risk Management for Pharmaceutical and Biotechnology Manufacturing Operations: Annex 2: Case Studies in the Manufacturing of Pharmaceutical Drug ProductsReport / Survey by Parenteral Drug Association, 11/01/2013

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    PDA TR 64Technical Report No. 64 (TR 64) Active Temperature-Controlled Systems: Qualification GuidanceReport / Survey by Parenteral Drug Association, 10/01/2013

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    PDA TR 33Technical Report 33, Revised 2013 (TR 33) Evaluation, Validation and Implementation of Alternative and Rapid Microbiological MethodsReport / Survey by Parenteral Drug Association, 10/01/2013

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    PDA TR 63Technical Report No. 63 (TR 63) Quality Requirements for the Extemporaneous Preparation of Clinical Trial MaterialsReport / Survey by Parenteral Drug Association, 09/01/2013

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    PDA TR 13Technical Report 13 Revised, (TR 13) Fundamentals of an Environmental Monitoring ProgramReport / Survey by Parenteral Drug Association, 06/01/2014

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