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14 CFR Part 39 - Airworthiness Directives CFM International S.A. CFM56–5B1/P, –5B2/ P, –5B3/P, –5B3/P1, –5B4/P, –5B5/P, –5B6/P, –5B7/P, –5B8/P, –5B9/P, –5B1/ 2P, –5B2/2P, –5B3/2P, –5B3/2P1, –5B4/ 2P, –5B4/P1, –5B6/2P, –5B4/2P1, and –5B9/2P Turbofan Engine
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Sterile Filtration of Pharmaceutical Products - Validation and Regulatory Requirements
By - Roger Cowan
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By - Roger Cowan
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FFIEC BSA/AML Examination Manual: What Compliance Officers Really Need to Know?
By - Doug Keipper
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By - Doug Keipper
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Technical Writing for the Pharmaceutical, Medical Device and Biotech Industries
By - Joy McElroy
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By - Joy McElroy
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Trial Master File and Clinical Data Management Regulated by FDA
By - Carolyn Troiano
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By - Carolyn Troiano
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Good Documentation Practice and Record Keeping Regulations (FDA & EMA)
By - Dr. Afsaneh Motamed Khorasani
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By - Dr. Afsaneh Motamed Khorasani
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Understanding and Preparing for FDA Pharmaceutical Inspections
By - Michael Ferrante
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By - Michael Ferrante
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