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False Claims Act Liability: A Guide for Drug and Device Manufacturers
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Equipment Maintenance, Cleaning and Calibration: A Guide to FDA Requirements
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Expediting the FDA Generic Drug Approval Process
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Environmental & Microbiological Monitoring at Drug Manufacturing Sites
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Equipment Design and Qualification: A Guide for Drug and Device Manufacturers
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Electronic Batch Recording and Batch Release for Drugmakers
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Electronic Document Management Systems for Drugmakers
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Effective Internal Audits and Quality Control Units for Devicemakers
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Efficient Premarket Applications: Three FDA Submission Paths That Require Less Time, Money and Effort
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$397.00
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Drugmakers' Guide to Global Quality API Manufacturing
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Drugmakers Guide to the 21st Century Cures Act: Changing the Face of Pharmaceutical and Biologics Regulation
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Drafting Clinical Trial Agreements: Using the Right Words and Phrases
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