10 CFR Part 430 - Energy Conservation Program for Consumer Products: Determination Concerning the Potential for Energy Conservation Standards for Non-Class A External Power Supplies
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Sterile Filtration of Pharmaceutical Products - Validation and Regulatory Requirements
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By - Roger Cowan
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FFIEC BSA/AML Examination Manual: What Compliance Officers Really Need to Know?
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By - Doug Keipper
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Technical Writing for the Pharmaceutical, Medical Device and Biotech Industries
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By - Joy McElroy
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Trial Master File and Clinical Data Management Regulated by FDA
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Good Documentation Practice and Record Keeping Regulations (FDA & EMA)
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By - Dr. Afsaneh Motamed Khorasani
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Understanding and Preparing for FDA Pharmaceutical Inspections
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By - Michael Ferrante
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